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
1986355887
Device Listing 1986355887
Listing Summary
#
Listing key
1986355887
Premarket submission
K160643
Device
ENROUTE 0.014 Guidewire
Applicant
Lake Region Medical
Product code
DQX
Decision date
2016-10-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
219886
3014526664
3007215228
SILK ROAD MEDICAL, INC.
1
Y
2020-04-25
1213 Innsbruck Drive Sunnyvale CA US 94089