# K093946: Hoveround Hoverglide Model Hoverglide MK-2

- Pathway: 510(k) (Traditional)
- Applicant: Hoveround Corp.
- Decided: Mar 22, 2010 after 89 days
- Product code: ILK (Transport, Patient, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5150
- 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 intended use is to assist transfer of an individual up or down a straight, residential, indoor staircase while in a seated position.

Source page: https://510kreport.com/device/K093946
Methodology: https://510kreport.com/methodology