# K881463: Multimode (TM) Power Module System

- Pathway: 510(k) (Traditional)
- Applicant: Dufco Electronics, Inc.
- Decided: Jul 18, 1988 after 102 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
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K983520: Breath Control (Breath Actuator), Sensitouch Breath Control, Head Array (Switch Head Control), Tri-Switch Head Array, HD (1998), 2 descendants of its own
- K073330: Freedom Sciences Motion Control Module (MCM) (2008), 1 descendant of its own
- K091723: Freedom Sciences Motion Control Module Version 1.5 (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K881463
Methodology: https://510kreport.com/methodology