K251828
- 510(k) number
- K251828
- Device name
- CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set
- Applicant
- Cerenovus, Inc. FL · US
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2025-08-22
- Date received
- 2025-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K251828.pdf
Official FDA record: K251828
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.