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

    MAXITHERM

    K Number: K811743 · Decision Jul 16, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    87
    Registration Numbers
    87
    Same Product Code
    154
    Applicant Total
    2
    Review Days
    27

    Basic Information

    Device Name
    MAXITHERM
    K Number
    K811743
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5900
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    CINCINNATI SUB-ZERO
    Date Received
    June 19, 1981
    Decision Date
    July 16, 1981
    Product Code
    DWJ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DWJ System, Thermal Regulating

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