K243193
- 510(k) number
- K243193
- Device name
- Cross Wise Multi-Use RF Adapter Cable
- Applicant
- Circa Scientific, Inc. CO · US
- Product code
- DXF — Catheter, Septostomy
- Decision date
- 2024-11-26
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K243193.pdf
Official FDA record: K243193
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.