# K981885: Sunrise Scooter Series, Model Unassigned, 3 Wheel Standard Model, 3 Wheel Mid Range Model, 3 Wheel High End Model, 4 Whe

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical, Inc.
- Decided: Nov 12, 1998 after 167 days
- Product code: INI (Vehicle, Motorized 3-Wheeled)
- Device class: 2
- Regulation: 21 CFR 890.3800
- 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 its predicate without a number.
- (no number) Quickie P190: named in the summary without a submission number
- (no number) Quickie P120: named in the summary without a submission number
- (no number) Sabre: named in the summary without a submission number
- (no number) Ranger II: named in the summary without a submission number

## Indications for use
Sunrise scooters empower physically challenged persons by providing a means of mobility.

Source page: https://510kreport.com/device/K981885
Methodology: https://510kreport.com/methodology