Medical Device Manufacturer · US , Arnold , MO

Bremed Italia, S.R.L. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

Total

Cleared

Denied

Bremed Italia, S.R.L. has 3 FDA 510(k) cleared medical devices. Based in Arnold, US.

Historical record: 3 cleared submissions from 1997 to 1998. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Bremed Italia, S.R.L. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bremed Italia, S.R.L.

3 devices

1-3 of 3