Class Class II
Visionbody (K222386)
Description
Visionbody by Vb Technologies AG, an FDA 510(k) cleared physical medicine device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222386
Clearance Date2023-02-24
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222386
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. Visionbody (K222386) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K213741 | TENS & EMS DEVICE (Model: FM-B2403A) | Shenzhen Jian Feng Electronic Techn... | 2022 |
| K190966 | Katalyst Training System | Katalyst, Inc. | 2020 |
| K180956 | Electrical Stimulator - Model R-C1 TENS and EMS stimulator,... | Shenzhen Roundwhale Technology Co. ... | 2018 |
Trace the full predicate network for K222386
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.