K260149
- 510(k) number
- K260149
- Device name
- Versus Catheter (VS110-9NB)
- Applicant
- Liquet Medical, Inc. VA · US
- Product code
- QEY — Mechanical Thrombolysis Catheter
- Decision date
- 2026-02-17
- Date received
- 2026-01-20
- 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: K260149.pdf
Official FDA record: K260149
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.