Midmark Corp.

Midmark Corp. — FDA 510(k) Submissions

Midmark Corp. has submitted 31 FDA 510(k) premarket notifications since 1981, of which 31 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilizer, Steam, Table, Examination, Medical, Powered, Unit, Examining/treatment, Ent, Stretcher, Wheeled, Table, Operating-room, Ac-powered . Use the specialty filter in the sidebar to narrow results.