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
1533465791
Device Listing 1533465791
Listing Summary
#
Listing key
1533465791
Premarket submission
K080131
Device
VPAP ST
Applicant
Resmed, Ltd.
Product code
BZD
Decision date
2008-04-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
12414
3004604967
3004604967
David Lanfranchi
1
N
2026-01-01
9001 Spectrum Center Blvd San Diego CA US 92123
101579
3007573469
1000115734
RESMED CORP
1
Y
2026-01-01
9001 Spectrum Center Boulevard San Diego CA US 92123