# K030254: Interferential Stimulator, Model RTM1000

- Pathway: 510(k) (Traditional)
- Applicant: Ryan Telemedicine
- Decided: Feb 26, 2003 after 33 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CS3101 Interferential Stimulator: named in the summary without a submission number

## Most influential descendants
- K042057: Infinity Electrotherapy System (2004), 0 descendants of its own

## Indications for use
The RTM1000 Electrotherapy device is a multifunction nerve stimulation device intended to be used for muscle and nerve stimulation using any one of its two therapy modes, Interferential Current Stimulation, Neuromuscular Electrical Stimulation. In the Interferential Current Mode the RTM1000 is indicated for the following conditions: Symptomatic relief of pain Symptomatic management and relief of chronic pain Adjunctive treatment for the management of post traumatic and post-surgical pain. In the Neuromuscular Stimulation Mode, the RTM1000 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 muscle to prevent venous thrombosis; and Maintaining or increasing range of motion.

Source page: https://510kreport.com/device/K030254
Methodology: https://510kreport.com/methodology