K241510
- 510(k) number
- K241510
- Device name
- CROSSLEAD Tracker
- Applicant
- Asahi Intecc Co., Ltd. JP
- Product code
- DQX — Wire, Guide, Catheter
- Decision date
- 2024-08-14
- Date received
- 2024-05-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241510.pdf
Official FDA record: K241510
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.