K241702
- 510(k) number
- K241702
- Device name
- CROSSLEAD 0.014inch
- Applicant
- Asahi Intecc Co., Ltd. JP
- Product code
- DQX — Wire, Guide, Catheter
- Decision date
- 2025-02-06
- Date received
- 2024-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K241702.pdf
Official FDA record: K241702
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.