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
1474458767
Device Listing 1474458767
Listing Summary
#
Listing key
1474458767
Premarket submission
K843927
Device
CT 9000
Applicant
General Electric Co.
Product code
JAK
Decision date
1984-12-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26605
9612283
3002808529
GE Healthcare Japan Corporation
1
N
2026-01-01
7-127, Asahigaoka 4-chome HINO-SHI Tokyo JP 191-8503