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510(k) Data Aggregation

    K Number
    K052836
    Device Name
    BODIHEALTH SYSTEM
    Manufacturer
    USA LASER THERAPEUTICS, INC.
    Date Cleared
    2007-02-13

    (495 days)

    Product Code
    GZJ
    Regulation Number
    882.5890
    Why did this record match?
    Applicant Name (Manufacturer) :

    USA LASER THERAPEUTICS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The BodiHealth System is intended for temporary symptomatic relief and management of chronic intractable pain and as an adjunctive treatment in the management of post-surgical and post-traumatic pain.
    Device Description
    Not Found
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