Medical Device Manufacturer · ES , Barcelona, Spain

Iberhospitex, S.A. - FDA 510(k) Cleared Devices

3 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Iberhospitex, S.A. has 1 FDA 510(k) cleared medical devices. Based in Barcelona, Spain, ES.

Historical record: 1 cleared submissions from 1988 to 1989. Primary specialty: General & Plastic Surgery.

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

Iberhospitex, S.A. is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Iberhospitex, S.A.

3 devices

1-3 of 3