K241244
- 510(k) number
- K241244
- Device name
- CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
- Applicant
- Cerenovus, Inc. FL · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2024-10-16
- Date received
- 2024-05-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K241244.pdf
Official FDA record: K241244
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.