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
1294269503
Device Listing 1294269503
Listing Summary
#
Listing key
1294269503
Premarket submission
K234141
Device
AISAP Cardio V1.0
Applicant
Aisap
Product code
POK
Decision date
2024-08-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
342487
3040335643
3040335643
AISAP LTD
1
N
2026-01-01
Sheba Road 2 Ramat Gan Central IL 5266202