K250665
- 510(k) number
- K250665
- Device name
- SKR 3000
- Applicant
- Konica Minolta, Inc. JP
- Product code
- MQB — Solid State X-Ray Imager (Flat Panel/Digital Imager)
- Decision date
- 2025-06-17
- Date received
- 2025-03-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K250665.pdf
Official FDA record: K250665
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.