Class Class II
Salix Coronary Plaque (V1.0.0) (K251837)
Description
Salix Coronary Plaque (V1.0.0) by Artrya Limited, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251837
Clearance Date2025-08-20
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251837
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. Salix Coronary Plaque (V1.0.0) (K251837) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243038 | Salix Central | Artrya Limited | 2025 |
| K242240 | CaRi-Plaque | Caristo Diagnostics , Ltd. | 2025 |
| K241038 | Cardiac CT Function Software Application | Circle Cardiovascular Imaging | 2024 |
Trace the full predicate network for K251837
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.