K251006
- 510(k) number
- K251006
- Device name
- NeVasc Aspiration System
- Applicant
- Vesalio, Inc. CA · US
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2025-11-10
- Date received
- 2025-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251006.pdf
Official FDA record: K251006
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.