Vitalograph (Ireland) , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Model 9160 VitaloQUB, Model 9100 PFT/DICO, Vitalograph Model 6000 Alpha
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vitalograph (Ireland) , Ltd. Cardiovascular ✕
1 devices