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
1855344991
Device Listing 1855344991
Listing Summary
#
Listing key
1855344991
Premarket submission
K052274
Device
GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000
Applicant
Guidant Corporation
Product code
GEI
Decision date
2005-09-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
82684
2242352
2242352
Maquet Cardiovascular LLC
1
Y
2026-01-01
45 BARBOUR POND DRIVE Wayne NJ US 07470