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
1659644433
Device Listing 1659644433
Listing Summary
#
Listing key
1659644433
Premarket submission
K213971
Device
Atrial Fibrillation History Feature
Applicant
Apple, Inc.
Product code
QDB
Decision date
2022-06-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
223004
3014343954
3014343954
APPLE INC.
1
N
2026-01-01
One Apple Park Way Cupertino CA US 95014