Medical Device Manufacturer · US , Redmond , WA

Vesiflo, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2014

1

Total

0

Cleared

1

Denied

Vesiflo, Inc. has 0 FDA 510(k) cleared medical devices. Based in Redmond, US.

Active since 2014. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Vesiflo, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vesiflo, Inc.

1 devices

1-1 of 1

Not Cleared Oct 14, 2014

INFLOW INTRAURETHRAL VALVE-PUMP

DEN130044 · PIH

Gastroenterology & Urology · 354d