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
1310249920
Device Listing 1310249920
Listing Summary
#
Listing key
1310249920
Premarket submission
K964746
Device
HISPEED CT/I WITH PERFORMIX TUBE AND WARP SCAN OPTION
Applicant
GE Medical Systems
Product code
JAK
Decision date
1997-01-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26607
2126677
2126677
GE MEDICAL SYSTEMS, LLC
1
Y
2026-01-01
3000 N GRANDVIEW BLVD. Waukesha WI US 53188