Medical Device Manufacturer · US , Ontario , CA

The Kipp Group - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1997

Total

Cleared

Denied

The Kipp Group has 6 FDA 510(k) cleared medical devices. Based in Ontario, US.

Historical record: 6 cleared submissions from 1997 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by The Kipp Group Filter by specialty or product code using the sidebar.

The Kipp Group 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 - The Kipp Group

6 devices

1-6 of 6