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
1130835122
Device Listing 1130835122
Listing Summary
#
Listing key
1130835122
Premarket submission
K172512
Device
ACRO HCG Pregnancy Rapid Test
Applicant
Acro Biotech, Inc.
Product code
LCX
Decision date
2018-02-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
154603
3005360469
3005670738
ACRO BIOTECH Inc.
1
N
2026-01-01
4650 Arrow Hwy Suite D6 Montclair CA US 91763