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
1643703022
Device Listing 1643703022
Listing Summary
#
Listing key
1643703022
Premarket submission
K242254
Device
D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter
Applicant
Dk Medical Technology Co., Ltd.
Product code
PNO
Decision date
2025-04-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
316566
3027343398
3027343398
James Wang
1
N
2026-01-01
30 N Gould St Unit 291 Sheridan WY US 82801