Honeywell, Inc.

Honeywell, Inc. — FDA 510(k) Submissions

Honeywell, Inc. has submitted 69 FDA 510(k) premarket notifications since 1976, of which 69 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrocardiograph, Recorder, Paper Chart, Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), Display, Cathode-ray Tube, Medical, Computer, Blood-pressure . Use the specialty filter in the sidebar to narrow results.