Medical Device Manufacturer · US , Stamford , CT

K. W. Griffen Co. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1987

Total

Cleared

Denied

K. W. Griffen Co. has 3 FDA 510(k) cleared medical devices. Based in Stamford, US.

Historical record: 3 cleared submissions from 1987 to 1996. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by K. W. Griffen Co. Filter by specialty or product code using the sidebar.

K. W. Griffen Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - K. W. Griffen Co.

4 devices

1-4 of 4