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

    STUDIODOP VICORDER

    K Number: K071730 · Decision Dec 20, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    16
    Registration Numbers
    16
    Same Product Code
    71
    Applicant Total
    1
    Review Days
    178

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    Basic Information

    Device Name
    STUDIODOP VICORDER
    K Number
    K071730
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    870.2880
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Skidmore Medical, Limited
    Date Received
    June 25, 2007
    Decision Date
    December 20, 2007
    Product Code
    JOP
    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
    JOP Transducer, Ultrasonic

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