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
1847155582
Device Listing 1847155582
Listing Summary
#
Listing key
1847155582
Premarket submission
K993141
Device
AT HOME QUICKCUP PREGNANCY TEST, MODEL 9015
Applicant
Phamatech
Product code
LCX
Decision date
1999-11-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
82571
2031229
3000719950
PHAMATECH INC.
1
N
2026-01-01
15175 Innovation Dr San Diego CA US 92128