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

    PHONOCARDIOGRAPH

    K Number: K924054 · Decision Jan 22, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    17
    Applicant Total
    6
    Review Days
    163

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    Basic Information

    Device Name
    PHONOCARDIOGRAPH
    K Number
    K924054
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    870.2390
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Echo Ultrasound
    Date Received
    August 12, 1992
    Decision Date
    January 22, 1993
    Product Code
    DQC
    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
    DQC Phonocardiograph

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