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.

Haemopharm Biofluids S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Haemopharm Biofluids S.R.L.

2 devices

1-2 of 2