K230726
- 510(k) number
- K230726
- Device name
- CEREGLIDE 92 Intermediate Catheter
- Applicant
- Cerenovus, Inc. FL · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2023-11-29
- Date received
- 2023-03-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K230726.pdf
Official FDA record: K230726
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.