# K990122: Independence 624

- Pathway: 510(k) (Traditional)
- Applicant: Eagle Parts & Products, Inc.
- Decided: Jun 25, 1999 after 163 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 2 (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 11, 2006 · Not classified · Z-0039-2007: The wheel hub bolts may loosen resulting in the wheels coming off.
- Jul 11, 2006 · Not classified · Z-0040-2007: The wheel hub bolts may loosen resulting in the wheels coming off.

## Indications for use
o ad 0 e Yevnporary of ?QTW\G\Y\QV\'*‘\% M\ O\O\\ \k’\v\ \ Y\ Po\\'eé\ Nawidua\ o meve abedt 1ndoore and outdoo “H\VOU%\’\ the vee g0 a bafirir'fiv% Powefe,& Wheeled device. we\a\/\% copacity ok NAnvrdual net 4o exceed 250 \be,

Source page: https://510kreport.com/device/K990122
Methodology: https://510kreport.com/methodology