Medical Device Manufacturer · US , Piscataway , NJ

Perimed, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

Total

Cleared

Denied

Perimed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Piscataway, US.

Historical record: 6 cleared submissions from 1989 to 1999. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Perimed, Inc.

6 devices

1-6 of 6