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

    TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET

    K Number: K102430 · Decision Sep 10, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    139
    Registration Numbers
    139
    Same Product Code
    104
    Applicant Total
    1
    Review Days
    15

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    Basic Information

    Device Name
    TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET
    K Number
    K102430
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2900
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Tyco Electronics Corporation
    Date Received
    August 26, 2010
    Decision Date
    September 10, 2010
    Product Code
    DSA
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    Y

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DSA Cable, Transducer And Electrode, Patient, (Including Connector)

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