Medical Device Manufacturer · US , Mchenry , IL

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

4 submissions · 4 cleared · Since 1981

Total

Cleared

Denied

Proto-Med, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1981 to 1984. Primary specialty: Anesthesiology.

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

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

4 devices

1-4 of 4