K254046
- 510(k) number
- K254046
- Device name
- BosCATH Support Catheter
- Applicant
- Sonorous NV, Inc. CA · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2026-04-21
- Date received
- 2025-12-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K254046.pdf
Official FDA record: K254046
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.