Class Class II
Spectral CT 7500 RT (K240844)
Description
Spectral CT 7500 RT by Philips Medical Systems Technologies , Ltd., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240844
Clearance Date2024-10-18
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240844
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. Spectral CT 7500 RT (K240844) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K203020 | Spectral CT | Philips Medical Systems Nederland B.V. | 2021 |
| K171850 | Philips CT Big Bore | Philips Medical Systems (Cleveland)... | 2017 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K244008 | Spectral CT | Philips Medical Systems Technologie... | 2025 |
Trace the full predicate network for K240844
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.