# K053284: Magbody DT-600

- Pathway: 510(k) (Traditional)
- Applicant: Durtech System Corp.
- Decided: Mar 10, 2006 after 105 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- 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.

## Indications for use
The DT-600 is a multifunction electrotherapy device with various treatment modes that allow for neuromuscular electrical stimulation (EMS) and transcutaneous electrical nerve stimulation (TENS). As a EMS device, DT-600 is indicated for the following conditions: * Relaxation of muscle spasms As a TENS device, the DT-600 is indicated for the following conditions: * For symptomatic relief of chronic intractable pain.

Source page: https://510kreport.com/device/K053284
Methodology: https://510kreport.com/methodology