Medical Device Manufacturer · US , Fort Washington , PA

Pilling Weck Surgical - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1998

Total

Cleared

Denied

Pilling Weck Surgical has 5 FDA 510(k) cleared medical devices. Based in Fort Washington, US.

Historical record: 5 cleared submissions from 1998 to 2000. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Pilling Weck Surgical Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pilling Weck Surgical

5 devices

1-5 of 5