Medical Device Manufacturer · US , Mountain View , CA

Percutaneous Systems, Incorporated - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2005

Total

Cleared

Denied

Percutaneous Systems, Incorporated has 5 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Historical record: 5 cleared submissions from 2005 to 2009. Primary specialty: Gastroenterology & Urology.

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

Percutaneous Systems, Incorporated 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, Incorporated

5 devices

1-5 of 5