# K042764: Medline Strider Midi 4

- Pathway: 510(k) (Special)
- Applicant: Medline Industries, Inc.
- Decided: Oct 8, 2004 after 3 days
- Product code: INI (Vehicle, Motorized 3-Wheeled)
- Device class: 2
- Regulation: 21 CFR 890.3800
- Recalls of this device: 1 (0 Class I)
- 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.

## Recalls of this device
- Jul 20, 2006 · Not classified · Z-1523-06: The P&G Solo 60A electronic control unit on the Midi Scooters may overheat.

## Indications for use
The intended use of the Medline Strider MIDI 4 scooter is to provide mobility to persons that have difficulty walking for prolonged periods of time. It is intended to increase the mobility of persons who are both physically and mentally capable of assessing and reacting to any driving situation. The Medline Strider MIDI 4 scooter is constructed for use both indoors and outdoors. It is for use indoors, on pavement, sidewalks, roads with the exception of crossing or pedestrian zones and areas free from motor traffic. It must not be driven on public roads except when no pavements are available.

Source page: https://510kreport.com/device/K042764
Methodology: https://510kreport.com/methodology