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
1903293863
Device Listing 1903293863
Listing Summary
#
Listing key
1903293863
Premarket submission
K042338
Device
CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE
Applicant
Lake Region Mfg., Inc.
Product code
DQX
Decision date
2004-09-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
35634
2126666
2126666
Lake Region Medical
1
Y
2026-01-01
340 Lake Hazeltine Dr CHASKA MN US 55318