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
1708549503
Device Listing 1708549503
Listing Summary
#
Listing key
1708549503
Premarket submission
K970823
Device
SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER
Applicant
Scimed Life Systems, Inc.
Product code
DQY
Decision date
1997-06-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26737
3004859241
3004859241
Aaron Dunbar
1
N
2026-01-01
300 Boston Scientific Way Marlborough MA US 01752