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
1458750825
Device Listing 1458750825
Listing Summary
#
Listing key
1458750825
Premarket submission
K102175
Device
RAPIDVUE HCG TEST
Applicant
Quidel Corporation
Product code
JHI
Decision date
2010-08-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
34107
3002792284
3002792284
LABORATORIOS SCANTIBODIES S.A. DE C.V.
1
N
2026-01-01
Calle Los Vinedos #4100 Parque Industrial El Bajio CP 21430 TECATE Baja California MX --
331806
3033507883
3033507883
Laboratorios Scantibodies, S.A. de C.V.
1
N
2026-01-01
Calle Camino Vecinal No. 6351, Valle Redondo Tijuana Baja California MX 22335