Medical Device Manufacturer · IT , Mirandola

Haemotronic S.P.A. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Haemotronic S.P.A. has 2 FDA 510(k) cleared medical devices. Based in Mirandola, IT.

Last cleared in 2021. Active since 2020. Primary specialty: General Hospital.

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

Haemotronic S.P.A. 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 - Haemotronic S.P.A.

2 devices

1-2 of 2