K233791
- 510(k) number
- K233791
- Device name
- Drivewire 24 Guidewire
- Applicant
- Rapid-Medical , Ltd. IL
- Product code
- MOF — Guide, Wire, Catheter, Neurovasculature
- Decision date
- 2024-07-11
- Date received
- 2023-11-28
- 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: K233791.pdf
Official FDA record: K233791
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.