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
1497561281
Device Listing 1497561281
Listing Summary
#
Listing key
1497561281
Premarket submission
K813495
Device
ALT (SGPT)
Applicant
Pointe Scientific, Inc.,
Product code
CKA
Decision date
1981-12-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
303263
3021841051
3021841051
BIALEX LAB
1
N
2026-01-01
717 Ohio Ave Wichita Falls TX US 76301