K243080
- 510(k) number
- K243080
- Device name
- Riptide Aspiration System
- Applicant
- Micro Therapeutics, Inc. d/b/a ev3 Neurovascular CA · US
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2024-10-29
- Date received
- 2024-09-30
- 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: K243080.pdf
Official FDA record: K243080
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.