Medical Device Manufacturer · US , Exton , PA

Kensey Nash Corporation - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2006

Total

Cleared

Denied

Kensey Nash Corporation has 6 FDA 510(k) cleared medical devices. Based in Exton, US.

Historical record: 6 cleared submissions from 2006 to 2013. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Kensey Nash Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kensey Nash Corporation

6 devices

1-6 of 6