Braemar Corp. - FDA 510(k) Cleared Devices
Recent clearances: DIGITRAKPLUS HOLTER RECORDER, DXP1000 HOLTER RECORDER, BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Braemar Corp. General Hospital ✕
1 devices