Medical Device Manufacturer · IT , Tovo Di S. Agata

Haemopharm Biofluids S.R.L. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Haemopharm Biofluids S.R.L. has 2 FDA 510(k) cleared medical devices. Based in Tovo Di S. Agata, IT.

Last cleared in 2021. Active since 2015. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Haemopharm Biofluids S.R.L.

2 devices

1-2 of 2