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
1298224757
Device Listing 1298224757
Listing Summary
#
Listing key
1298224757
Premarket submission
K151901
Device
AirView
Applicant
Resmed, Ltd.
Product code
CBK
Decision date
2015-11-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
101579
3007573469
1000115734
RESMED CORP
1
Y
2026-01-01
9001 Spectrum Center Boulevard San Diego CA US 92123