K Number
K040193
Device Name
MODEL GST-1
Date Cleared
2004-04-27

(90 days)

Product Code
Regulation Number
882.5890
Panel
NE
Reference & Predicate Devices
N/A
Predicate For
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

AS A POWERED MUSCLE STIMULATOR

    1. Relaxation of muscle spasms
  • Prevention or retardation of disuse atrophy 2 .
  • Increasing local blood circulation
    1. Muscle re-education
  • Immediate post-surgical stimulation of calf muscles to 5. prevent venous thrombosis
    1. Maintaining or increasing range of motion

AS A TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR

  • 1 . Symptomatic relief of chronic intractable pain
Device Description

Not Found

AI/ML Overview

The provided document is a 510(k) premarket notification letter from the FDA for a device named GST-1, which functions as a Transcutaneous Electrical Nerve Stimulator (TENS) and a Powered Muscle Stimulator.

This document does not contain information regarding acceptance criteria, device performance, study details, sample sizes, ground truth establishment, or expert qualifications for a study. The letter only confirms that the FDA has reviewed the submission and determined that the device is substantially equivalent to legally marketed predicate devices for the stated indications for use.

Therefore, I cannot provide the requested information based on the given text.

To answer your request, clinical study reports or summaries, often found within the 510(k) submission itself (which is typically a much larger document than this letter), would be needed. This FDA letter is a regulatory approval notice, not a scientific study report.

§ 882.5890 Transcutaneous electrical nerve stimulator for pain relief.

(a)
Identification. A transcutaneous electrical nerve stimulator for pain relief is a device used to apply an electrical current to electrodes on a patient's skin to treat pain.(b)
Classification. Class II (performance standards).