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
1750376071
Device Listing 1750376071
Listing Summary
#
Listing key
1750376071
Premarket submission
K221655
Device
Multiflex Steerable Sheath
Applicant
Vizaramed, Inc.
Product code
DYB
Decision date
2022-11-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
317693
3027366703
3027366703
VIZARAMED, INC.
1
N
2026-01-01
1914 O'Toole Way San Jose CA US 95131