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
1529075856
Device Listing 1529075856
Listing Summary
#
Listing key
1529075856
Premarket submission
K111617
Device
PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1
Applicant
Acare Technology Co., Ltd.
Product code
DQA
Decision date
2011-12-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
25740
3006395447
3006395447
Daniel Kamm
1
N
2026-01-01
8870 Ravello Ct Naples FL US 34114