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

    3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE

    K Number: K020365 · Decision May 3, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    41
    Applicant Total
    5
    Review Days
    88

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    Basic Information

    Device Name
    3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE
    K Number
    K020365
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    870.4200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    3t Medical Systems, LLC
    Date Received
    February 4, 2002
    Decision Date
    May 3, 2002
    Product Code
    KRI
    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
    KRI Accessory Equipment, Cardiopulmonary Bypass

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