Mem Medical, Inc.

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

Mem Medical, Inc. has submitted 27 FDA 510(k) premarket notifications since 1979, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Attachment, Intermittent Mandatory Ventilation (imv), Valve, Non-rebreathing, Nebulizer (direct Patient Interface), Tubing, Pressure And Accessories, Mouthpiece, Breathing . Use the specialty filter in the sidebar to narrow results.