Utah Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UTAH CVX-RIPE, FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+), BT-CATH
38
Total
38
Cleared
0
Denied
FDA 510(k) Regulatory Record - Utah Medical Products, Inc. Orthopedic ✕
2 devices