Medical Device Manufacturer · US , St. Paul , MN

Omni-Tract Surgical, Div. Minn. Scientific, Inc. - FDA 510(k) Cleared...

4 submissions · 4 cleared · Since 1992
4
Total
4
Cleared
0
Denied

Omni-Tract Surgical, Div. Minn. Scientific, Inc. has 4 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Historical record: 4 cleared submissions from 1992 to 2000. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Omni-Tract Surgical, Div. Minn. Scientific, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Omni-Tract Surgical, Div. Minn. Scientific, Inc.
4 devices
1-4 of 4
Filters