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

    VITALINE 2

    K Number: K822856 · Decision Jul 29, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    305

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    Basic Information

    Device Name
    VITALINE 2
    K Number
    K822856
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    American Heartline, Inc.
    Date Received
    September 27, 1982
    Decision Date
    July 29, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

    Other Clearances by American Heartline, Inc.

    K Number Device Name
    K812695 DISK