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510(k) Data Aggregation

    K Number
    K012140
    Device Name
    COM-PATCH
    Manufacturer
    Date Cleared
    2001-10-05

    (87 days)

    Product Code
    Regulation Number
    882.1320
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Apex self-adhesive electrodes are intended to be used in TENS (Transcutaneous Electrical Stimulation) and NMES (NeuroMuscular Electrical Stimulation) applications.

    Device Description

    Com-Patch, Self Adhesive Electrodes Models: AP-0981201, AP-0981203, AP-0981208, and AP-0981209

    AI/ML Overview

    I am sorry, but based on the provided text, there is no information about acceptance criteria or a study proving the device meets acceptance criteria. The document is an FDA 510(k) clearance letter for "Com-Patch, Self Adhesive Electrodes," which states that the device is substantially equivalent to legally marketed predicate devices.

    The letter discusses:

    • The device name and models
    • Regulation number, name, and class
    • Product codes
    • The date the 510(k) was filed and received
    • Confirmation of substantial equivalence based on indications for use
    • Regulatory requirements and contacts for further information

    It does NOT include:

    1. A table of acceptance criteria or reported device performance
    2. Sample sizes or data provenance for any test sets
    3. Information about experts or ground truth establishment
    4. Adjudication methods
    5. Multi-reader multi-case (MRMC) comparative effectiveness studies
    6. Standalone algorithm performance
    7. Type of ground truth used
    8. Sample size for training sets
    9. How ground truth for training sets was established

    The document's purpose is to grant market clearance based on substantial equivalence, not to detail the results of performance studies against specific acceptance criteria.

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