Medical Device Manufacturer · IT , Campli

Pentaferte Italia S.R.L. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pentaferte Italia S.R.L. General Hospital ✕
1 devices
1-1 of 1
Cleared Jul 20, 2022
Pentaflush
K214080 · NGT
General Hospital · 205d
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All3 Gastroenterology & Urology 2 General Hospital 1