# K993298: E Z Chair

- Pathway: 510(k) (Traditional)
- Applicant: Premier Designs
- Decided: Nov 16, 1999 after 46 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
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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The EZ Chair will be used, like a Sunrise Medical Quickie 2 HP wheelchair in the Hemi Height position, to aid the temporarily or permanently mobility impaired individual to move about indoors, and outdoors, through the use of a wheeled device (wheelchair). You can propel yourself by pushing along the ground with your feet or you can propel yourself by pushing the pedals. Like a Hemi Height chair, the EZ Chair will be used by people with limited use of their legs due to conditions such as: Arthritis, Single leg Amputee, Multiple Sclerosis, Muscular Dystrophy, Hemiplegic, Parkinson’s Disease, Emphysema, Geriatric, Cerebral Palsy, Head Injury, Post Polio, etc.

Source page: https://510kreport.com/device/K993298
Methodology: https://510kreport.com/methodology