Puritan Bennett Corp.

Puritan Bennett Corp. — FDA 510(k) Submissions

Puritan Bennett Corp. has submitted 110 FDA 510(k) premarket notifications since 1976, of which 101 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Continuous, Facility Use, Ventilator, Emergency, Manual (resuscitator), Unit, Liquid-oxygen, Portable, Ventilator, Non-continuous (respirator), Attachment, Breathing, Positive End Expiratory Pressure . Use the specialty filter in the sidebar to narrow results.