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

    SALTZMAN STETHOSCOPE HEAD

    K Number: K854771 · Decision May 9, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    185
    Registration Numbers
    185
    Same Product Code
    27
    Applicant Total
    3
    Review Days
    161

    Basic Information

    Device Name
    SALTZMAN STETHOSCOPE HEAD
    K Number
    K854771
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    870.1875
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    K & S MEDICORP
    Date Received
    November 29, 1985
    Decision Date
    May 9, 1986
    Product Code
    LDE
    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
    LDE Stethoscope, Manual

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