Surgistar, Inc.

Surgistar, Inc. — FDA 510(k) Submissions

Surgistar, 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 Keratome, Ac-powered, Scalpel, One-piece, Laparoscope, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.