Storz Medical AG - FDA 510(k) Cleared Devices
Recent clearances: Storz Medical MAGNETOLITH Muscle Stimulator, Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece, D-Actor 200 Vibration Massage System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Storz Medical AG General & Plastic Surgery ✕
1 devices