Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K020130
    Date Cleared
    2002-12-02

    (321 days)

    Product Code
    Regulation Number
    890.5850
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ROLOR POWERED MUSCLE STIMULATOR, MODEL GP-8016M

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Specific indications: used to apply an electrical current to electrodes on a patient's skin to function as: Relaxation of muscle spasms. Prevention or retardation of disuse atrophy Increasing local blood circulation. Maintaining or increasing range of motion.

    Device Description

    ROLOR POWERED MUSLCE STIMULATOR GP-8016M

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA regarding a powered muscle stimulator. It does not contain any information about acceptance criteria, study details, or device performance data. Therefore, I cannot fulfill the request to describe the acceptance criteria and the study that proves the device meets them based on the given input.

    The document primarily focuses on:

    • The FDA's determination of substantial equivalence for the "ROLOR POWERED MUSCLE STIMULATOR GP-8016M".
    • The classification of the device (Class II - Product Code: IPF).
    • General regulatory requirements for the device.
    • The intended use of the device, which includes relaxation of muscle spasms, prevention or retardation of disuse atrophy, increasing local blood circulation, and maintaining or increasing range of motion.

    No performance data, study designs, sample sizes, expert qualifications, or ground truth methodologies are mentioned.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1