MUSCLEMAX PLUS ELECTRICAL MUSCLE STIMULATOR
Device Facts
| Record ID | K962462 |
|---|---|
| Device Name | MUSCLEMAX PLUS ELECTRICAL MUSCLE STIMULATOR |
| Applicant | Smith and Nephew Donjoy, Inc. |
| Product Code | IPF · Physical Medicine |
| Decision Date | Sep 23, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 890.5850 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
The MuscleMax™ Plus is a disposable single patient use EMS (Electrical Muscle Stimulator) intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.
Device Story
Disposable single-patient use EMS; delivers electrical currents to muscles via skin-contact electrodes. Input: user-adjusted intensity via recessed dial. Operation: 2200Hz biphasic symmetrical signal in 72 pps bursts; 20-second ON/OFF cycle. Output: muscle contraction. Indicators: green LED (ON/active), yellow LED (OFF cycle). Power: four 1.5V DC batteries. Safety: non-removable strain-relieved leads; recessed controls prevent accidental adjustment. Used by patients or clinicians to facilitate muscle contraction.
Clinical Evidence
Bench testing only. Verified maximum charge per pulse (75μC) across 500, 2K, and 10K Ohm loads. Functional battery life confirmed to exceed 100 hours at maximum intensity.
Technological Characteristics
Disposable EMS; 2200Hz biphasic symmetrical waveform; 72 pps burst frequency. Powered by 4x 1.5V DC batteries. Includes recessed intensity dial, green/yellow LED status indicators, and non-removable strain-relieved leads. Uses pre-gelled conductive electrode pads.
Indications for Use
Indicated for patients requiring muscle contraction via electrical stimulation to the body area. Contraindications: none stated.
Regulatory Classification
Identification
A powered muscle stimulator is an electrically powered device intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.
Reference Devices
- pre-gelled conductive electrode pads (K912461)
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