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
1037402823
Device Listing 1037402823
Listing Summary
#
Listing key
1037402823
Premarket submission
K904524
Device
CAPTIA(R) SYPHILIS M, MODIFICATION
Applicant
Mercia Diagnostics , Ltd.
Product code
LIP
Decision date
1990-12-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
16364
1318354
1318354
Trinity Biotech USA
1
Y
2026-01-01
2823 Girts Rd Jamestown NY US 14701