Group items tagged #FDA - Diigo Community

FDA proposes new rules for mammography services - 0 views

www.medicaldevice-network.com/...proposes-new-mammography-rules

#FDA_New_Proposes #Food_and_Drug_Administration ##Breast_Cancer #FDA #Mammography_Services #Improve_The_Quality

shared by jacob logan on 01 Apr 19 - No Cached

jacob logan on 01 Apr 19

The US Food and Drug Administration (FDA) has proposed a new policy intended to modernise and improve the quality of mammography, which is used for breast cancer screening and diagnosis.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has proposed a new policy intended to modernise and improve the quality of mammography, which is used for breast cancer screening and diagnosis.</div>

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AngioDynamics to study NanoKnife in pancreatic cancer - 0 views

www.medicaldevice-network.com/...oknife-pancreatic-cancer-study

#Angio_Dynamics #Pancreatic_Cancer #Nanoknife_System #FDA #Food_and_Drug_Administration #investigational_Device_Exemption

shared by jacob logan on 03 Apr 19 - No Cached

jacob logan on 03 Apr 19

AngioDynamics has received approval from the US Food and Drug Administration (FDA) for an investigational device exemption (IDE) application of its NanoKnife System in the treatment of stage III pancreatic cancer.

<div class="cArrow"> </div><div class="cContentInner">AngioDynamics has received approval from the US Food and Drug Administration (FDA) for an investigational device exemption (IDE) application of its NanoKnife System in the treatment of stage III pancreatic cancer.</div>

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FDA approves Innoblative's radiofrequency ablation device - 0 views

www.medicaldevice-network.com/...ive-designs-rf-ablation-device

#Food_and_Drug_Administration #FDA #US_FOod #Radio_Frequency #Radio_Frequency_Ablation_Device #Electrosurgical_Device

shared by jacob logan on 12 Apr 19 - No Cached

jacob logan on 12 Apr 19

The US Food and Drug Administration (FDA) has granted clearance to Innoblative Designs' electrosurgical device SIRA RFA.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has granted clearance to Innoblative Designs' electrosurgical device SIRA RFA.</div>

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FDA clears NeuroSigma's Monarch device to treat ADHD - 0 views

www.medicaldevice-network.com/...clears-neurosigma-monarch-adhd

#US_FOOD_And_Drug_Administration #FDA #Neurosigma_Monarch_Device #External_trigeminal_Nerve_Stimulation #Attention_Deficit_Hyperactivity_disorder #ADHD

shared by jacob logan on 24 Apr 19 - No Cached

jacob logan on 24 Apr 19

The US Food and Drug Administration (FDA) has granted marketing clearance for Monarch, an external trigeminal nerve stimulation (eTNS) system developed by NeuroSigma, to treat attention deficit hyperactivity disorder (ADHD).

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has granted marketing clearance for Monarch, an external trigeminal nerve stimulation (eTNS) system developed by NeuroSigma, to treat attention deficit hyperactivity disorder (ADHD).</div>

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Boston Scientific gets FDA approval for LOTUS Edge system - 0 views

www.medicaldevice-network.com/...ientific-lotus-edge-system-nod

#Boston_Scientific #FDA #Food_and_Drug_Administration #Lotus_Adge #US_Food #Lotus_Adge_System

shared by jacob logan on 25 Apr 19 - No Cached

jacob logan on 25 Apr 19

Boston Scientific has received the US Food and Drug Administration (FDA) approval for the use of LOTUS Edge Aortic Valve System to treat severe aortic stenosis.

<div class="cArrow"> </div><div class="cContentInner">Boston Scientific has received the US Food and Drug Administration (FDA) approval for the use of LOTUS Edge Aortic Valve System to treat severe aortic stenosis.</div>

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FDA warns against use of surgical robots for cancer surgeries - 0 views

www.medicaldevice-network.com/...siste-surgical-devices-warning

#surgical_robots #cancer_surgeries #FDA #doctors

shared by jacob logan on 05 Mar 19 - No Cached

jacob logan on 05 Mar 19

The US Food and Drug Administration (FDA) has highlighted concerns about using robotically assisted surgical devices for mastectomies and other cancer surgeries, citing a lack of evidence for safety and effectiveness.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has highlighted concerns about using robotically assisted surgical devices for mastectomies and other cancer surgeries, citing a lack of evidence for safety and effectiveness.</div>

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For persistent depression FDA approves a novel treatment based on ketamine - 0 views

www.latimes.com/...ssion-drug-20190305-story.html

depression fda novel treatment based

shared by Bobby Brown on 06 Mar 19 - No Cached

Bobby Brown on 06 Mar 19

For people with intractable depression, the FDA has approved a nasal spray called esketamine, which can take effect in hours, compared to weeks or months for traditional treatments. Esketamine is a component of ketamine, which has been used as a party drug.

<div class="cArrow"> </div><div class="cContentInner">For people with intractable depression, the FDA has approved a nasal spray called esketamine, which can take effect in hours, compared to weeks or months for traditional treatments. Esketamine is a component of ketamine, which has been used as a party drug.</div>

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Paige.AI gets breakthrough status for cancer diagnosis solution - 0 views

www.medicaldevice-network.com/...ge-ai-breakthrough-designation

#Artificial_Intelligence #Cancer_Diagnosis #Cancer #AI #Device #US_Food #FDA

shared by jacob logan on 13 Mar 19 - No Cached

jacob logan on 13 Mar 19

Paige.AI has received breakthrough device designation from the US Food and Drug Administration (FDA) for a cancer diagnosis solution based on artificial intelligence (AI).

<div class="cArrow"> </div><div class="cContentInner">Paige.AI has received breakthrough device designation from the US Food and Drug Administration (FDA) for a cancer diagnosis solution based on artificial intelligence (AI).</div>

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FDA approves Xvivo Perfusion System in lung transplant - 0 views

www.medicaldevice-network.com/...pproves-xvivo-perfusion-system

#FDA #Xvivo_Perfusion_System #Food_And_Durg_Administration #Lung_Trasplant

shared by jacob logan on 30 Apr 19 - No Cached

jacob logan on 30 Apr 19

Steen Solution Perfusate to heSwedish medical technology firm Xvivo Perfusion has received the US Food and Drug Administration (FDA) approval for the use of its Xvivo Perfusion System with lp in lung transplant procedure.

<div class="cArrow"> </div><div class="cContentInner">Steen Solution Perfusate to heSwedish medical technology firm Xvivo Perfusion has received the US Food and Drug Administration (FDA) approval for the use of its Xvivo Perfusion System with lp in lung transplant procedure.</div>

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Medtronic's Attain Stability left heart lead receives FDA approval - 0 views

www.medicaldevice-network.com/...-attain-stability-gets-fda-nod

#Medtronics_Attain_Stability #heart_Lead #FDA #Food_and_Drug_Administration #US_Food #Precise_Lead_Placement

shared by jacob logan on 06 May 19 - No Cached

jacob logan on 06 May 19

The US Food and Drug Administration (FDA) has granted approval to Medtronic's Attain Stability Quad MRI SureScan left heart lead. The device is the only active-fixation left heart lead, and is designed for precise lead placement and stability.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has granted approval to Medtronic's Attain Stability Quad MRI SureScan left heart lead. The device is the only active-fixation left heart lead, and is designed for precise lead placement and stability.</div>

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FDA approves Gore Tag Conformable Thoracic Stent Graft - 0 views

www.medicaldevice-network.com/...gore-tag-conformable-fda-nod

#FDA #Food_and_Drug_Administration #Gore_Tag_Conformable #Material_Sciences_Company

shared by jacob logan on 20 May 19 - No Cached

jacob logan on 20 May 19

Material sciences company W. L. Gore & Associates has received approval from the US Food and Drug Administration (FDA) for its Tag Conformable Thoracic Stent Graft, a thoracic endovascular aortic repair (TEVAR) device.

<div class="cArrow"> </div><div class="cContentInner">Material sciences company W. L. Gore & Associates has received approval from the US Food and Drug Administration (FDA) for its Tag Conformable Thoracic Stent Graft, a thoracic endovascular aortic repair (TEVAR) device.</div>

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FDA approves Cochlear Nucleus Profile Plus Series implant - 1 views

www.medicaldevice-network.com/...us-profile-plus-series-implant

#Food_and_Drug_Administration #Cochlear_Nucleus #Series_Implant #Us_Food #FDA

shared by jacob logan on 19 Jun 19 - No Cached

jacob logan on 19 Jun 19

The US Food and Drug Administration (FDA) has approved the new Cochlear Nucleus Profile Plus Series Cochlear Implant and the Nucleus 7 Sound Processor's new built-in connectivity.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has approved the new Cochlear Nucleus Profile Plus Series Cochlear Implant and the Nucleus 7 Sound Processor's new built-in connectivity.</div>

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Magnetic hearing devices may interfere with shunt systems, says FDA - 1 views

www.medicaldevice-network.com/...ear-implant-shunt-interference

#Magnetic_Hearing_Device #Shunt_System #FDA #US_Food #Food_and_Drug_Administration #Cerebrospinal_Fluid #Hearing_Device

shared by jacob logan on 19 Jul 19 - No Cached

jacob logan on 19 Jul 19

The US Food and Drug Administration (FDA) has issued a statement warning healthcare providers about potential complications in patients fitted with both programmable cerebrospinal fluid (CSF) shunt systems and certain magnetic hearing devices.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has issued a statement warning healthcare providers about potential complications in patients fitted with both programmable cerebrospinal fluid (CSF) shunt systems and certain magnetic hearing devices.</div>

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Utah lab gets FDA go-ahead on COVID-19 test, ready to produce 50K daily - 0 views

www.deseret.com/...y-co-diagnostics-utah-pandemic

utah lab gets fda test ready produce daily news

shared by Bobby Brown on 20 Mar 20 - No Cached

Bobby Brown on 20 Mar 20

Utah molecular diagnostics company Co-Diagnostics has earned emergency U.S. Food and Drug Administration approval of its COVID-19 test, which it hopes will increase testing in the coronavirus outbreak.

<div class="cArrow"> </div><div class="cContentInner">Utah molecular diagnostics company Co-Diagnostics has earned emergency U.S. Food and Drug Administration approval of its COVID-19 test, which it hopes will increase testing in the coronavirus outbreak.</div>

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Bobby Brown on 20 Mar 20

Utah molecular diagnostics company Co-Diagnostics has earned emergency U.S. Food and Drug Administration approval of its COVID-19 test, which it hopes will increase testing in the coronavirus outbreak.

<div class="cArrow"> </div><div class="cContentInner">Utah molecular diagnostics company Co-Diagnostics has earned emergency U.S. Food and Drug Administration approval of its COVID-19 test, which it hopes will increase testing in the coronavirus outbreak.</div>

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FDA labels Ethicon surgical staplers recall as Class I - 1 views

www.medicaldevice-network.com/...fda-ethicon-staplers-recall

#FDA #Food_and_Drug_Administration #FDA_Labels #Ethicon_Surgical_Staplers #US_Food #Johnson #High_RIsk

shared by jacob logan on 21 May 19 - No Cached

jacob logan on 21 May 19

The US Food and Drug Administration (FDA) has labelled a recall of circular staplers by Johnson & Johnson (J&J) unit Ethicon as Class I, or high risk.

<div class="cArrow"> </div><div class="cContentInner">The US Food and Drug Administration (FDA) has labelled a recall of circular staplers by Johnson & Johnson (J&J) unit Ethicon as Class I, or high risk.</div>

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A quality portal for a healthcare company by Mamsys - 0 views

Healthcare digitalhealth fda development portal

shared by mamsys-world on 19 Dec 22 - No Cached

mamsys-world on 19 Dec 22

A quality portal for a healthcare company processing thousands of patient and provider data and having multiple features For more such exciting project updates keep following Mamsys or write to us at info@mamsys.com

<div class="cArrow"> </div><div class="cContentInner">A quality portal for a healthcare company processing thousands of patient and provider data and having multiple features For more such exciting project updates keep following Mamsys or write to us at info@mamsys.com</div>

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