Medical Device Manufacturer · US , Washington, Dc , DC

Percutaneous Systems, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2004

Total

Cleared

Denied

Percutaneous Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 6 cleared submissions from 2004 to 2011. Primary specialty: Gastroenterology & Urology.

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

Percutaneous Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Percutaneous Systems, Inc.

6 devices

1-6 of 6