Simpson/Basye, Inc.

Simpson/Basye, Inc. — FDA 510(k) Submissions

Simpson/Basye, Inc. has submitted 12 FDA 510(k) premarket notifications since 1978, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tenaculum, Uterine, Electrocautery, Gynecologic (and Accessories), Applicator, Absorbent Tipped, Non-sterile, Instrument, Manual, Specialized Obstetric-gynecologic, Tray, Surgical, Instrument . Use the specialty filter in the sidebar to narrow results.