Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1567502629
Device Listing 1567502629
Listing Summary
#
Listing key
1567502629
Premarket submission
K071011
Device
MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDER
Applicant
Braemar, Inc.
Product code
MWJ
Decision date
2007-04-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15639
2133409
1000520785
BRAEMAR MANUFACTURING, LLC
1
N
2020-04-25
1285 Corporate Center Dr Ste 150 EAGAN MN US 55121