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
2037858453
Device Listing 2037858453
Listing Summary
#
Listing key
2037858453
Premarket submission
K883664
Device
LUM VASCULAR PROCEDURE SYSTEM #B5200A
Applicant
General Electric Co.
Product code
IYB
Decision date
1988-11-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26609
9611343
1000284313
Tracey Holevas
1
N
2026-01-01
3000 N. Grandview BLVD Waukesha WI US 53188