Medical Device Manufacturer · US , Rye , NY

Perlink USA, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1990

Total

Cleared

Denied

Perlink USA, Inc. has 6 FDA 510(k) cleared medical devices. Based in Rye, US.

Historical record: 6 cleared submissions from 1990 to 1993. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Perlink USA, Inc.

6 devices

1-6 of 6