# K053285: Magbody DT-1200, DT-1200T, DT-1200M, DT-1200PT, DT-1200PM

- Pathway: 510(k) (Traditional)
- Applicant: Durtech System Corp.
- Decided: Jan 5, 2006 after 41 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
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-1200 series 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, (available for DT-1200, DT-1200M and DT-1200PM) the DT-1200 is indicated for the following conditions: * Relaxation of muscle spasms * Prevention or retardation of disuse atrophy * Increasing local blood circulation * Muscle re-education * Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis * Maintaining or increasing range of motion As a TENS device, (available for DT-1200, DT-1200T and DT-1200PT) the DT-1200 is indicated for the following conditions: * Symptomatic relief and management of chronic, intractable pain * Adjunctive treatment for post-surgical and post-trauma acute pain

Source page: https://510kreport.com/device/K053285
Methodology: https://510kreport.com/methodology