The Timeter Group

The Timeter Group — FDA 510(k) Submissions

The Timeter Group has submitted 4 FDA 510(k) premarket notifications since 1985, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Electric For Gravity Flow Infusion Systems, Regulator, Pressure, Gas Cylinder, Humidifier, Non-direct Patient Interface (home-use), Flowmeter, Tube, Thorpe, Back-pressure Compensated . Use the specialty filter in the sidebar to narrow results.