Medical Device Manufacturer · US , Middletown , NY

Repro-Med Systems, Inc. - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1985

Total

Cleared

Denied

Repro-Med Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in Middletown, US.

Historical record: 5 cleared submissions from 1985 to 2011. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Repro-Med Systems, Inc.

6 devices

1-6 of 6