Omni-Tract Surgical, Div. Minn. Scientific, Inc.

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

Omni-Tract Surgical, Div. Minn. Scientific, Inc. has submitted 4 FDA 510(k) premarket notifications since 1992, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stripper, Artery, Intraluminal, Laparoscope, General & Plastic Surgery, Arthroscope, Retractor . Use the specialty filter in the sidebar to narrow results.