Westmed Intl.

Westmed Intl. — FDA 510(k) Submissions

Westmed Intl. has submitted 9 FDA 510(k) premarket notifications since 1993, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filter, Bacterial, Breathing-circuit, Flowmeter, Calibration, Gas, Generator, Oxygen, Portable, Attachment, Breathing, Positive End Expiratory Pressure, Balloon, Epistaxis . Use the specialty filter in the sidebar to narrow results.