K253589
- 510(k) number
- K253589
- Device name
- Liberant RX Aspiration Catheter
- Applicant
- Medtronic Interventional Vascular, Inc. MA · US
- Product code
- QEZ — Aspiration Thrombectomy Catheter
- Decision date
- 2026-04-23
- Date received
- 2025-11-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253589.pdf
Official FDA record: K253589
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.