Medical Device Manufacturer · US , Morton Grove , IL

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

4 submissions · 4 cleared · Since 1999

Total

Cleared

Denied

Medifix, Inc. has 4 FDA 510(k) cleared medical devices. Based in Morton Grove, US.

Historical record: 4 cleared submissions from 1999 to 2001. Primary specialty: Gastroenterology & Urology.

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

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

4 devices

1-4 of 4