Medical Device Manufacturer · US , Whitefish Bay , WI

Cytophil, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2008

Total

Cleared

Denied

Cytophil, Inc. has 8 FDA 510(k) cleared medical devices. Based in Whitefish Bay, US.

Historical record: 8 cleared submissions from 2008 to 2015. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Cytophil, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cytophil, Inc.

8 devices

1-8 of 8