Medical Device Manufacturer · IT , Mirandola

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

2 submissions · 2 cleared · Since 2020
2
Total
2
Cleared
0
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.

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