Medical Device Manufacturer · US , Burnsville , MN

Braemar Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

5

Total

5

Cleared

0

Denied

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

4 devices

1-4 of 4

Cleared Mar 28, 2003

ER800 SERIES ECG EVENT RECORDER

Cardiovascular · 10d

Cleared Nov 24, 1999

DIGITRAKPLUS HOLTER RECORDER

Cardiovascular · 29d

Cleared Nov 24, 1999

DXP1000 HOLTER RECORDER

Cardiovascular · 29d

Cleared Apr 12, 1995

BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER

Cardiovascular · 175d