Medical Device Manufacturer · US , Mchenry , IL

W.G. Whitney Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1977

Total

Cleared

Denied

W.G. Whitney Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1977 to 1984. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by W.G. Whitney Corp. Filter by specialty or product code using the sidebar.

W.G. Whitney Corp. 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 - W.G. Whitney Corp.

7 devices

1-7 of 7