K232542
- 510(k) number
- K232542
- Device name
- Wedge XL Delivery Catheter
- Applicant
- MicroVention, Inc. CA · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2024-05-16
- Date received
- 2023-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232542.pdf
Official FDA record: K232542
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.