K262398
- 510(k) number
- K262398
- Device name
- CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set
- Applicant
- CERENOVUS, Inc. FL · US
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2026-08-13
- Date received
- 2026-07-14
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K262398.pdf
Official FDA record: K262398
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.