Analogic Corp. - FDA 510(k) Cleared Devices
Recent clearances: SYNERAD OMNI, MODELS AN6255 AND AN6265, SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600, LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P
32
Total
32
Cleared
0
Denied
FDA 510(k) Regulatory Record - Analogic Corp. Anesthesiology ✕
1 devices