BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MAGNATHERM MODEL 1000 SS

    K Number: K934151 · Decision Feb 17, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    44
    Applicant Total
    2
    Review Days
    541

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    Basic Information

    Device Name
    MAGNATHERM MODEL 1000 SS
    K Number
    K934151
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5290
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Intl. Medical Electronics , Ltd.
    Date Received
    August 25, 1993
    Decision Date
    February 17, 1995
    Product Code
    IMJ
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

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    Other Clearances by Intl. Medical Electronics , Ltd.

    K Number Device Name
    K771540 MAGNATHERM 2000