# K042535: Adventure A10

- Pathway: 510(k) (Traditional)
- Applicant: Ulrich Alber GmbH
- Decided: Oct 5, 2004 after 15 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K900565 (1990). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993413: Storm Series, Power 9000 Series and Power Tiger with Gyroscope Control, Invacare Corp. (1999) Summary page 1.

## Indications for use
A wheelchair can be provided as a result of medical indication where walking is no longer possible or the ability to walk is severely restricted through: * paralysis * loss of a limb or limbs * defects/deformation of a limb or limbs * contractures of the joints · other illnesses The intended use of the wheelchair is to provide mobility to persons limited to a sitting position, that have the capability of operating a powered wheelchair

Source page: https://510kreport.com/device/K042535
Methodology: https://510kreport.com/methodology