Class Class II
AV Viewer (K250181)
Description
AV Viewer by Philips Medical Systems Nederland B.V., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250181
Clearance Date2025-07-15
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250181
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. AV Viewer (K250181) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K173588 | Illumeo System | Philips Medical Systems Technologie... | 2018 |
| K163711 | IQon Spectral CT | Philips Medical Systems (Cleveland)... | 2017 |
| K162025 | IntelliSpace Portal Platform | Philips Medical Systems Nederlands ... | 2016 |
Trace the full predicate network for K250181
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.