# K981558: Mycycle Handmaster, Light

- Pathway: 510(k) (Traditional)
- Applicant: Richvale, Ltd.
- Decided: Jul 9, 1998 after 69 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: 1 generation back to K880280 (1988). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K880280: Breezy Wheelchair, Motion Designs, Inc. (1988) Summary page 1.
- (no number) Wijit manual power attachment: named in the summary without a submission number

## Indications for use
The intended use of the device is as a wheelchair. The wheelchair and drive system empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions in all ages, including but not limited to Arthritis, paraplegic, Quadriplegic, Multiple Sclerosis and other immobilizing or debilitating conditions. Our device and the predicate device provide the same function for occupants who are unable to move due to injuries or other medical conditions.

Source page: https://510kreport.com/device/K981558
Methodology: https://510kreport.com/methodology