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See today's BioWorld MedTech
Home » Fist Assist earns FDA breakthrough device designation for wearable vein dilation device
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Fist Assist earns FDA breakthrough device designation for wearable vein dilation device

Dec. 16, 2021
By Annette Boyle
Fist Assist Devices LLC received a breakthrough device designation from the FDA for its Fist Assist Model FA-1 device for patients with end-stage renal disease (ESRD). The pre-surgical dilation device promotes arteriovenous (AV) fistula creation in renal failure patients with inadequate vein size for creation of an AV fistula for hemodialysis. An AV fistula is a surgical connection between an artery and a vein used as an access point for dialysis.
BioWorld MedTech Regulatory Nephrology Wearable FDA

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