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
1629563572
Device Listing 1629563572
Listing Summary
#
Listing key
1629563572
Premarket submission
K190472
Device
Aptima CV/TV Assay
Applicant
Hologic, Inc.
Product code
PQA
Decision date
2019-05-16
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