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
1860137594
Device Listing 1860137594
Listing Summary
#
Listing key
1860137594
Premarket submission
K973991
Device
METRON QA-510 SPO2 ANALYZER
Applicant
Metron U.S., Inc.
Product code
DQA
Decision date
1998-01-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17366
2921581
2921581
FLUKE BIOMEDICAL
1
Y
2026-01-01
6920 SEAWAY BLVD. EVERETT WA US 98203