K242776
- 510(k) number
- K242776
- Device name
- LimFlow V-Ceiver
- Applicant
- LimFlow, Inc. CA · US
- Product code
- MMX — Device, Percutaneous Retrieval
- Decision date
- 2025-02-14
- Date received
- 2024-09-13
- 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: K242776.pdf
Official FDA record: K242776
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.