BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ULTICARE 2500 TREATMENT CHAIR

    K Number: K791016 · Decision Jun 27, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    26

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    Basic Information

    Device Name
    ULTICARE 2500 TREATMENT CHAIR
    K Number
    K791016
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6140
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    American Health Care Industries, Inc.
    Date Received
    June 1, 1979
    Decision Date
    June 27, 1979
    Product Code
    FRK
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FRK Chair, Examination And Treatment

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