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
1778987790
Device Listing 1778987790
Listing Summary
#
Listing key
1778987790
Premarket submission
K121182
Device
VIALOK NON-VENTED
Applicant
Yukon Medical, LLC
Product code
LHI
Decision date
2012-05-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
23594
2016493
2016493
CareFusion 303, INC.
1
Y
2026-01-01
10020 Pacific Mesa Blvd SAN DIEGO CA US 92121