K233917
- 510(k) number
- K233917
- Device name
- ICHOR 7F Embolectomy System (ICH-7F)
- Applicant
- Ichor FL · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2024-07-18
- Date received
- 2023-12-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K233917.pdf
Official FDA record: K233917
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.