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
2001082101
Device Listing 2001082101
Listing Summary
#
Listing key
2001082101
Premarket submission
K070462
Device
XPERT MRSA
Applicant
Cepheid
Product code
NQX
Decision date
2007-04-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72454
3004530258
3004530258
CEPHEID
1
N
2026-01-01
904 CARIBBEAN DRIVE Sunnyvale CA US 94089
303576
3016838963
3016838963
Cepheid
1
Y
2026-01-01
121 N Guild Ave 1175 S Guild Avenue Lodi CA US 95240