Medical Device Manufacturer · US , Riverside , CA

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

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

Stackhouse, Inc. has 4 FDA 510(k) cleared medical devices. Based in Riverside, US.

Historical record: 4 cleared submissions from 1994 to 2000. Primary specialty: General Hospital.

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

Stackhouse, Inc. 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 - Stackhouse, Inc.

4 devices

1-4 of 4