Medikmark, Inc.

Medikmark, Inc. — FDA 510(k) Submissions

Medikmark, Inc. has submitted 8 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 Drape, Surgical, Instrument, Manual, General Obstetric-gynecologic, Wrap, Sterilization, Tube Tracheostomy And Tube Cuff, Set, Administration, Intravascular . Use the specialty filter in the sidebar to narrow results.