# K092793: Modification to:Kneehab XP Conductive Garment, Model 411

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Medical Research, Ltd.
- Decided: Dec 7, 2009 after 87 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K912178 (1991). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083105: Kneehab XP Conductive Garment, Type 411, Bio-Medical Research, Ltd. (2009) Summary page 1.
- K091317: Lumbofix Conductive Garment, Model 420 Back, Bio-Medical Research, Ltd. (2009) Summary page 1.

## Indications for use
The Neurotech Kneehab Conductive Garment and associated accessories are indicated for use with Neurotech Stimulators to facilitate the frequent and correct positioning and repositioning of large, multiple, and/or difficult to reach stimulation sites associated with the quadriceps area of the leg.

Source page: https://510kreport.com/device/K092793
Methodology: https://510kreport.com/methodology