K233982
- 510(k) number
- K233982
- Device name
- CEREGLIDE 92 Catheter System
- Applicant
- Cerenovus, Inc. FL · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2024-05-09
- Date received
- 2023-12-18
- 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: K233982.pdf
Official FDA record: K233982
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.