Aequitron Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR, MODEL LP-1000 VOLUME VENTILATOR, OXYGEN CONCENTRATION INDICATOR
24
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aequitron Medical, Inc. General Hospital ✕
1 devices