# K943789: Power Wheelchair Conversion Kit

- Pathway: 510(k) (Traditional)
- Applicant: Alber Technologies, Inc.
- Decided: Nov 8, 1994 after 97 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K123769: ZX-I Power Add on (2013), 0 descendants of its own

## Recalls of this device
- Aug 1, 2004 · Not classified · Z-0803-05: may short circuit within the interface due to long term exposure of liquid
- Aug 1, 2004 · Not classified · Z-0804-05: may short circuit within the interface due to long term exposure of liquid

Source page: https://510kreport.com/device/K943789
Methodology: https://510kreport.com/methodology