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
1644954697
Device Listing 1644954697
Listing Summary
#
Listing key
1644954697
Premarket submission
K171816
Device
Kardia Band System
Applicant
AliveCor, Inc.
Product code
DXH
Decision date
2017-11-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
143789
3009715978
3009715978
AliveCor
1
N
2026-01-01
189 N Bernardo Avenue Suite 100 Mountain View CA US 94043