Hospitak, Inc.

Hospitak, Inc. — FDA 510(k) Submissions

Hospitak, Inc. has submitted 27 FDA 510(k) premarket notifications since 1978, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Condenser, Heat And Moisture (artificial Nose), Chamber, Oxygen, Topical, Extremity, Mask, Oxygen, Low Concentration, Venturi, Nebulizer (direct Patient Interface), Connector, Airway (extension) . Use the specialty filter in the sidebar to narrow results.