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
1018538090
Device Listing 1018538090
Listing Summary
#
Listing key
1018538090
Premarket submission
K802569
Device
ABNORMAL HEMOGLOBIN CONTROL
Applicant
Marilyn L. Amick
Product code
KHG
Decision date
1980-11-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
76880
1825740
1825740
Analytical Control Systems
1
N
2026-01-01
9058 Technology Drive Fishers IN US 46038