Southmedic, Inc.

Southmedic, Inc. — FDA 510(k) Submissions

Southmedic, Inc. has submitted 10 FDA 510(k) premarket notifications since 1984, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Vaporizer, Anesthesia, Non-heated, Analyzer, Gas, Carbon-dioxide, Gaseous-phase, Nebulizer (direct Patient Interface), Connector, Airway (extension) . Use the specialty filter in the sidebar to narrow results.