Medical Device Manufacturer · US , Burnsville , MN

Braemar Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Recent clearances: ER800 SERIES ECG EVENT RECORDER, DIGITRAKPLUS HOLTER RECORDER, DXP1000 HOLTER RECORDER

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Braemar Corp. General Hospital ✕

1 devices

1-1 of 1

Cleared Sep 28, 1998

BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720

General Hospital · 164d