K234034
- 510(k) number
- K234034
- Device name
- VenaCore Thrombectomy Catheter (46-101)
- Applicant
- Inari Medical, Inc. CA · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2024-02-09
- Date received
- 2023-12-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K234034.pdf
Official FDA record: K234034
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.