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
1173718251
Device Listing 1173718251
Listing Summary
#
Listing key
1173718251
Premarket submission
K002212
Device
MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608
Applicant
Micro Therapeutics, Inc.
Product code
DQX
Decision date
2000-08-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
83279
8020889
3003382061
Kae Miller
1
N
2026-01-01
200 Medtronic Drive Lafayette CO US 80026