Medical Device Manufacturer · US , Chicago , IL

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

8 submissions · 4 cleared · Since 1992

Total

Cleared

Denied

Medikmark, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 4 cleared submissions from 1992 to 1995. Primary specialty: General Hospital.

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

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

8 devices

1-8 of 8