K251789
- 510(k) number
- K251789
- Device name
- EMBOTRAP III Revascularization Device
- Applicant
- Neuravi Limited IE
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2025-09-25
- Date received
- 2025-06-11
- 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: K251789.pdf
Official FDA record: K251789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.