K252213
- 510(k) number
- K252213
- Device name
- Bendit17 Microcatheter
- Applicant
- Bend IT Technologies, Ltd. IL
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2025-12-03
- Date received
- 2025-07-15
- 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: K252213.pdf
Official FDA record: K252213
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.