Medical Device Manufacturer · US , Walker , MI

Stackhouse Assoc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1979

Total

Cleared

Denied

Stackhouse Assoc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 5 cleared submissions from 1979 to 1991. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Stackhouse Assoc.

5 devices

1-5 of 5