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
1068292366
Device Listing 1068292366
Listing Summary
#
Listing key
1068292366
Premarket submission
K213857
Device
HeartFlow Analysis
Applicant
HeartFlow, Inc.
Product code
PJA
Decision date
2022-10-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
302618
3021637148
3021637148
HEARTFLOW, INC.
1
N
2026-01-01
135 Main St Ste 1000 San Francisco CA US 94105