Haemopharm Biofluids S.R.L. is one of 205 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Haemopharm Biofluids S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: HMB32 Dialysis Solution, HMB32
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Haemopharm Biofluids S.R.L.
2 devices