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

    SKINTACT

    K Number: K024264 · Decision Jan 16, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    2
    Review Days
    24

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    Basic Information

    Device Name
    SKINTACT
    K Number
    K024264
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Leonhard Lang Co.
    Date Received
    December 23, 2002
    Decision Date
    January 16, 2003
    Product Code
    DRX
    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
    DRX Electrode, Electrocardiograph

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