Nova-Ventrx

Nova-Ventrx — FDA 510(k) Submissions

Nova-Ventrx has submitted 12 FDA 510(k) premarket notifications since 1981, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Tubing And Support, Ventilator (w Harness), Humidifier, Respiratory Gas, (direct Patient Interface), Valve, Non-rebreathing, Ventilator, Emergency, Manual (resuscitator), Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer . Use the specialty filter in the sidebar to narrow results.