Class Class II
Symbia Pro.specta VA20A Family (K231102)
Description
Symbia Pro.specta VA20A Family by Siemens Medical Solutions USA, Inc., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK231102
Clearance Date2023-05-17
Clearance TypeSpecial
Product CodeKPS
Regulation Number892.1200
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K231102
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. Symbia Pro.specta VA20A Family (K231102) cites 0 predicate devices and is itself cited by 1 later device.
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243186 | Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (1136... | Siemens Medical Solutions USA, Inc. | 2024 |
Trace the full predicate network for K231102
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.