Medical Device Manufacturer · US , Mchenry , IL

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

8 submissions · 6 cleared · Since 1977

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 1977 to 1980. Primary specialty: Cardiovascular.

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

Medcor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8