K241962
- 510(k) number
- K241962
- Device name
- Crossloop
- Applicant
- Asahi Intecc Co., Ltd. JP
- Product code
- DQX — Wire, Guide, Catheter
- Decision date
- 2025-03-27
- Date received
- 2024-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K241962.pdf
Official FDA record: K241962
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.