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
1809426043
Device Listing 1809426043
Listing Summary
#
Listing key
1809426043
Premarket submission
P940034
Device
GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)
Applicant
GEN-PROBE, INC.
Product code
MWA
Decision date
1995-12-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
147172
2024800
2024800
Hologic, Inc.
1
Y
2026-01-01
10210 Genetic Center Dr SAN DIEGO CA US 92121