Class Class II
PanopticAI Vital Signs (K240890)
Description
PanopticAI Vital Signs by PanopticAI technologies Limited, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240890
Clearance Date2024-12-23
Clearance TypeTraditional
Product CodeQME
Regulation Number870.2785
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240890
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. PanopticAI Vital Signs (K240890) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K211906 | Vital Signs | Oxehealth Limited | 2021 |
Trace the full predicate network for K240890
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.