Class Class II
Neuro20 Pro System (K223797)
Description
Neuro20 Pro System by Neuro20 Technologies, an FDA 510(k) cleared physical medicine device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223797
Clearance Date2023-02-23
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223797
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. Neuro20 Pro System (K223797) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201975 | miha bodytec II | Miha Bodytec GmbH | 2021 |
| K090632 | COMPEX REHAB | Chattanooga Group | 2009 |
Trace the full predicate network for K223797
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.