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
1010963956
Device Listing 1010963956
Listing Summary
#
Listing key
1010963956
Premarket submission
K962353
Device
ACCUSIGN DOA 5 (THC/OPI/COC/MET OR AMP/PCP)
Applicant
Princeton BioMeditech Corp.
Product code
DIO
Decision date
1996-08-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
6703
2246703
2246703
PRINCETON BIOMEDITECH CORP.
1
N
2026-01-01
4242 U.S. Hwy. 1 Monmouth Jct NJ US 08852