K251603
- 510(k) number
- K251603
- Device name
- Tigertriever 17 Ultra Revascularization Device
- Applicant
- Rapid Medical Ltd. IL
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2025-10-06
- Date received
- 2025-05-27
- 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: K251603.pdf
Official FDA record: K251603
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.