Westmed, Inc.

Westmed, Inc. — FDA 510(k) Submissions

Westmed, Inc. has submitted 8 FDA 510(k) premarket notifications since 1995, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Analyzer, Gas, Carbon-dioxide, Gaseous-phase, Intra-pulmonary Percussive Vibration (ipv) Devices, Monitor, Airway Pressure (includes Gauge And/or Alarm), Mask, Oxygen, Pump, Infusion, Elastomeric . Use the specialty filter in the sidebar to narrow results.