K260188
- 510(k) number
- K260188
- Device name
- LimFlow Vector
- Applicant
- LimFlow, Inc. CA · US
- Product code
- MGZ — Valvulotome
- Decision date
- 2026-03-18
- Date received
- 2026-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K260188.pdf
Official FDA record: K260188
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.