K232298
- 510(k) number
- K232298
- Device name
- DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl
- Applicant
- Canon, Inc. JP
- Product code
- OWB — Interventional Fluoroscopic X-Ray System
- Decision date
- 2024-04-26
- Date received
- 2023-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232298.pdf
Official FDA record: K232298
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.