Medical Device Manufacturer · US , Libertyville , IL

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

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Numedtec, Inc. has 2 FDA 510(k) cleared medical devices. Based in Libertyville, US.

Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Gastroenterology & Urology.

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

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

2 devices

1-2 of 2