Valley West, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 3600 PRESURE INFUSOR, SIGMACON 3600, LAPRO FLOW 3000, TRUMP-IT II AND MAGNUM 250
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Valley West, Inc. General Hospital ✕
2 devices