# K200583: Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL

- Pathway: 510(k) (Traditional)
- Applicant: Ki Mobility, LLC
- Decided: Sep 5, 2023 after 1,278 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K941989 (1994). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181090: Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs, Invacare Corporation (2018) Summary page 4.
- K123975: Quickie & Zippie Series, Sunrise Medical (2013) Summary page 4.

## Indications for use
The Ki Mobility Focus CR manual wheelchair is a manually operated device with wheels that is intended to provide mobility to adults restricted to a sitting position.

Source page: https://510kreport.com/device/K200583
Methodology: https://510kreport.com/methodology