Class Class
NeuroTrac® MyoPlus Pro (MYO120U) (K243079)
Description
NeuroTrac® MyoPlus Pro (MYO120U) by Verity Medical , Ltd., an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class
510(k) NumberK243079
Clearance Date2025-06-26
Clearance TypeTraditional
FDA Database
View on FDA DatabasePredicate lineage for K243079
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. NeuroTrac® MyoPlus Pro (MYO120U) (K243079) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201290 | Medline DeNovo 4Pro Electrical Stimulation Device | Medline Industries, Inc. | 2020 |
| K083704 | NUTRAC PELVATOR, MODEL PEL 200 | Verity Scientific , Ltd. | 2009 |
Trace the full predicate network for K243079
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.