# K210920: iBOT Personal Mobility Device (iBOT PMD)

- Pathway: 510(k) (Traditional)
- Applicant: Mobius Mobility
- Decided: Jun 16, 2021 after 79 days
- Product code: IMK (Wheelchair, Stair Climbing)
- Device class: 2
- Regulation: 21 CFR 890.3890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to P020033/S002 (2005). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172601: Next Generation iBOT, Deka Research & Development Corp. (2018) Summary page 4.

## Most influential descendants
- K243442: iBOT® PMD (2025), 0 descendants of its own

## Indications for use
The iBOT® Personal Mobility Device ("iBOT® PMD") is intended to provide indoor and outdoor mobility to persons restricted to a sitting position who meet the requirements of the user assessment and training certification program. The device allows for the option to climb stairs. Companions who are required to provide assistance during Assisted Stair Climbing Mode must meet the requirements of the training certification program. The iBOT® Personal Mobility Device ("iBOT® PMD") Occupied Transport option is indicated for providing persons, unable to transfer from their wheelchair into a standard factory motor vehicle seat, the option for transportation while seated in their iBOT® PMD wheelchair.

Source page: https://510kreport.com/device/K210920
Methodology: https://510kreport.com/methodology