Neoforce Group, Inc.

Neoforce Group, Inc. — FDA 510(k) Submissions

Neoforce Group, Inc. has submitted 7 FDA 510(k) premarket notifications since 2006, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Attachment, Breathing, Positive End Expiratory Pressure, Ventilator, Emergency, Manual (resuscitator), Incubator, Neonatal, Ventilator, Emergency, Powered (resuscitator), Monitor, Airway Pressure (includes Gauge And/or Alarm) . Use the specialty filter in the sidebar to narrow results.