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
FDA 510(k) Regulatory Record - Haemotronic S.P.A. General Hospital ✕
2 devices
1-2 of 2
Cleared Aug 19, 2021
Empty EVA Bag
K210749 · KPE
General Hospital · 160d
Cleared Jul 22, 2020
Empty EVA Bag
K193528 · KPE
General Hospital · 216d
Filters
Filter by Specialty
All2 General Hospital 2