Mega Medical, Inc.

Mega Medical, Inc. — FDA 510(k) Submissions

Mega Medical, Inc. has submitted 7 FDA 510(k) premarket notifications since 1991, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Anesthesia Conduction Kit, Catheter, Percutaneous, Needle, Hypodermic, Single Lumen, Drape, Surgical, Catheter, Intravascular, Diagnostic . Use the specialty filter in the sidebar to narrow results.