Class Class II
Brainomix 360 Triage Stroke (K251983)
Description
Brainomix 360 Triage Stroke by Brainomix Limited, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251983
Clearance Date2025-08-26
Clearance TypeTraditional
Product CodeQAS
Regulation Number892.2080
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251983
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 Triage Stroke (K251983) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232496 | Brainomix 360 Triage Stroke | Brainomix Limited | 2023 |
| K231837 | Brainomix 360 Triage LVO | Brainomix Limited | 2023 |
| K231656 | Brainomix 360 e-MRI | Brainomix Limited | 2023 |
| K231195 | Brainomix 360 Triage ICH | Brainomix Limited | 2023 |
| K223555 | Brainomix 360 e-CTP | Brainomix Limited | 2023 |
Trace the full predicate network for K251983
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.