Class Class II
Digital Radiography CXDI-CS01 (K230175)
Description
Digital Radiography CXDI-CS01 by Canon, Inc., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK230175
Clearance Date2023-02-15
Clearance TypeSpecial
Product CodeMQB
Regulation Number892.1680
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K230175
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Digital Radiography CXDI-CS01 (K230175) cites 1 predicate device and is itself cited by 2 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222661 | Digital Radiography CXDI-CS01 | Canon, Inc. | 2022 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241980 | !M1 | Solutions For Tomorrow AB | 2025 |
| K242515 | uDR 380i Pro | Shanghai United Imaging Healthcare ... | 2024 |
Trace the full predicate network for K230175
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.