# K090632: Compex Rehab

- Pathway: 510(k) (Traditional)
- Applicant: Chattanooga Group
- Decided: Jun 1, 2009 after 84 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- 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 K031077 (2003). 2 ancestors in all.
28 later devices descend from it; 3 cite it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071431: Globus Genesy 1100 Stimulator, Domino S.R.L. (2007) Summary page 1.

## Most influential descendants
- K124016: Empi Phoenix (2013), 25 descendants of its own
- K153704: Strive (2016), 24 descendants of its own
- K170903: Compex Wireless USA (2017), 10 descendants of its own
- K182203: JKH Stimulator Plus (2019), 7 descendants of its own
- K191151: JKH Stimulator Plus (2019), 4 descendants of its own

## Indications for use
The Compex® Rehab is an adjunctive multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (NMES). The Compex® Rehab is indicated for the following conditions: * Re-educating muscles * Relaxation of muscle spasm * Increasing local blood circulation * Retarding or preventing disuse atrophy * Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K090632
Methodology: https://510kreport.com/methodology