Class Class II
iBOT® PMD (K243442)
Description
iBOT® PMD by Mobius Mobility, an FDA 510(k) cleared physical medicine device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243442
Clearance Date2025-01-30
Clearance TypeTraditional
Product CodeIMK
Regulation Number890.3890
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243442
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. iBOT® PMD (K243442) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K210920 | iBOT Personal Mobility Device (iBOT PMD) | Mobius Mobility | 2021 |
| K150574 | Modular Power Positioning System | Motion Concepts | 2015 |
Trace the full predicate network for K243442
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.