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
1480435104
Device Listing 1480435104
Listing Summary
#
Listing key
1480435104
Premarket submission
K232017
Device
ARK Methotrexate II Assay
Applicant
Ark Diagnostics, Inc.
Product code
LAO
Decision date
2023-12-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
95995
3005755244
3005755244
ARK DIAGNOSTICS INC
1
N
2026-01-01
48089 Fremont Blvd Fremont CA US 94538