Medical Device Manufacturer · US , Flagstaff , AZ

Geon Corporation

3 submissions · 3 cleared · Since 2010
3
Total
3
Cleared
0
Denied

Geon Corporation — FDA 510(k) Submissions

Geon Corporation has submitted 3 FDA 510(k) premarket notifications since 2010, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Portable, Aspiration (manual Or Powered), Continuous Measurement Thermometer . Use the specialty filter in the sidebar to narrow results.

3 devices
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All3 Ear, Nose, Throat 2 General Hospital 1