Beacon Laboratories, Inc.

Beacon Laboratories, Inc. — FDA 510(k) Submissions

Beacon Laboratories, Inc. has submitted 18 FDA 510(k) premarket notifications since 1989, of which 18 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Apparatus, Electrosurgical, Electrosurgical Device, Insufflator, Laparoscopic . Use the specialty filter in the sidebar to narrow results.