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
1693128054
Device Listing 1693128054
Listing Summary
#
Listing key
1693128054
Premarket submission
K954256
Device
ANTI-TPO
Applicant
Biomerica, Inc.
Product code
JNL
Decision date
1995-11-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
76175
1222302
1000121039
American Laboratory Products Company
1
Y
2026-01-01
26 Keewaydin Drive Unit G Salem NH US 03079