Rusch, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RUSCH MMG/O'NEIL CATHETER, RUSCH EMERGENCY MASK, RUSCH MANUAL RESUSCITATOR BAG
26
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Rusch, Inc. General & Plastic Surgery ✕
1 devices