# K101611: Relay Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Dalton Instrument Corp.
- Decided: Sep 29, 2010 after 113 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The intended use of the Relay is to provide mobility to persons limited to a seated position that are capable of operating a powered wheelchair.

Source page: https://510kreport.com/device/K101611
Methodology: https://510kreport.com/methodology