Skytron, Div. the Kmw Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AURORA LED SERIES SURGICAL LIGHTS, STELLAR SERIES SURGICAL LIGHTS WITH HERMES, STELLAR
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Skytron, Div. the Kmw Group, Inc. Neurology ✕
1 devices