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
1538943513
Device Listing 1538943513
Listing Summary
#
Listing key
1538943513
Premarket submission
K243305
Device
Masimo W1
Applicant
Masimo Corporation
Product code
DPS
Decision date
2025-04-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
178837
3011353843
3011353843
MASIMO CORPORATION
1
N
2026-01-01
52 Discovery Irvine CA US 92618