Class Class II
VIVIX-M (K241113)
Description
VIVIX-M by Vieworks Co., Ltd., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241113
Clearance Date2025-01-16
Clearance TypeTraditional
Product CodeMUE
Regulation Number892.1715
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241113
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. VIVIX-M (K241113) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K170930 | RSM 2430C | DRTECH Corporation | 2017 |
Trace the full predicate network for K241113
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.