Gyrus Acmi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POWERSEAL Open Extended Jaw Sealer and Divider, Double-Action (PS-0021EJDA), RenaFlex Single-use Flexible Ureteroscope (SUURF-V Standard), POWERSEAL Sealer and Divider
42
Total
42
Cleared
0
Denied
FDA 510(k) Regulatory Record - Gyrus Acmi, Inc. General Hospital ✕
3 devices