Dideco S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: D731 MICRO 20 AND D733 MICRO 40 PEDIATRIC ARTERIAL FILTERS, D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR AND D 903 AVANT 2 PH.I.S.I.O. ADULT HOLLOW FIBER OXYGENATOR WITH COATING, D735 MICRO 20 AND D736 MICRO 40 NEWBORN-INFANT ARTERIAL FILTERS
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dideco S.P.A. Anesthesiology ✕
2 devices