Class Class II
Brainomix 360 e-CTP (K223555)
Description
Brainomix 360 e-CTP by Brainomix Limited, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223555
Clearance Date2023-06-01
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223555
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. Brainomix 360 e-CTP (K223555) cites 2 predicate devices and is itself cited by 3 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K180161 | Viz CTP | Viz. Ai, Inc. | 2018 |
| K121447 | ISCHEMA VIEW RAPID | Ischemaview, Inc. | 2013 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251983 | Brainomix 360 Triage Stroke | Brainomix Limited | 2025 |
| K243294 | Brainomix 360 e-ASPECTS | Brainomix Limited | 2025 |
| K223553 | Spine Planning (2.0), Elements Spine Planning, Elements Pla... | Brainlab AG | 2023 |
Trace the full predicate network for K223555
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.