Braemar, Inc. is one of 22012 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Braemar, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM, BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER, DL900 SERIES HOLTER RECORDER
5
Total
5
Cleared
0
Denied
Braemar, Inc. has 5 FDA 510(k) cleared medical devices. Based in Burnsville, US.
Historical record: 5 cleared submissions from 2004 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Braemar, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Braemar, Inc.
5 devices
Cleared
Jul 31, 2008
BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM
Cardiovascular
70d
Cleared
Oct 03, 2007
BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER
Cardiovascular
72d
Cleared
Jul 24, 2007
DL900 SERIES HOLTER RECORDER
Cardiovascular
28d
Cleared
Apr 27, 2007
MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDER
Cardiovascular
17d
Cleared
Oct 06, 2004
BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER
Cardiovascular
23d