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
1644442965
Device Listing 1644442965
Listing Summary
#
Listing key
1644442965
Premarket submission
K153335
Device
AlertWatch: OR
Applicant
Alertwatch, LLC
Product code
MWI
Decision date
2016-03-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
170986
3010895352
3010895352
ALERTWATCH, INC.
1
N
2020-04-25
330 E Liberty St Fl 4 Ann Arbor MI US 48104