K242254
- 510(k) number
- K242254
- Device name
- D·Kutting LL Peripheral Scoring Balloon Dilatation Catheter
- Applicant
- Dk Medical Technology Co., Ltd. CN
- Product code
- PNO — Catheter, Percutaneous, Cutting/Scoring
- Decision date
- 2025-04-21
- Date received
- 2024-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242254.pdf
Official FDA record: K242254
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.