Class Class II
Vibrant System (K223031)
Description
Vibrant System by Vibrant, Ltd., an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223031
Clearance Date2023-01-13
Clearance TypeTraditional
Product CodeQTN
Regulation Number876.5940
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223031
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. Vibrant System (K223031) 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 |
|---|---|---|---|
| K232830 | Vibrant System | Vibrant, Ltd. | 2023 |
Trace the full predicate network for K223031
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.