Quinton, Inc.

Quinton, Inc. — FDA 510(k) Submissions

Quinton, Inc. has submitted 164 FDA 510(k) premarket notifications since 1976, of which 160 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrocardiograph, Catheter, Percutaneous, Treadmill, Powered, Catheter, Peritoneal, Long-term Indwelling, Catheter, Subclavian . Use the specialty filter in the sidebar to narrow results.