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.

Cytophil, Inc. is one of 15016 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8