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
1022153674
Device Listing 1022153674
Listing Summary
#
Listing key
1022153674
Premarket submission
K082846
Device
APK SPO2 PULSE OXIMETER SENSOR
Applicant
APK Technology Co., Ltd.
Product code
DQA
Decision date
2009-04-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72122
9614500
3000225562
S.L.P. LTD.
1
N
2026-01-01
62 Anilevitz St. Tel-Aviv Tel Aviv IL 6706016