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
1300497029
Device Listing 1300497029
Listing Summary
#
Listing key
1300497029
Premarket submission
K013857
Device
AIMSTEP PREGNANCY
Applicant
Germaine Laboratories, Inc.
Product code
DHA
Decision date
2002-01-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
53892
1649661
3001451797
GERMAINE LABORATORIES, INC.
1
N
2026-01-01
11030 Wye Drive SAN ANTONIO TX US 78217