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
1542985462
Device Listing 1542985462
Listing Summary
#
Listing key
1542985462
Premarket submission
K811110
Device
MODELS: 52-01-0, 52-01-1
Applicant
Y
Product code
FPA
Decision date
1981-06-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
256720
3012410077
3012410077
CAREFUSION
1
Y
2026-01-01
3750 Torrey View Court San Diego CA US 92130