Precision Medical, Inc.

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

Precision Medical, Inc. has submitted 30 FDA 510(k) premarket notifications since 1984, of which 30 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Portable, Aspiration (manual Or Powered), Flowmeter, Tube, Thorpe, Back-pressure Compensated, Compressor, Air, Portable, Generator, Oxygen, Portable, Regulator, Pressure, Gas Cylinder . Use the specialty filter in the sidebar to narrow results.