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

    DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELEC

    K Number: K850132 · Decision Apr 9, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    191
    Registration Numbers
    191
    Same Product Code
    328
    Applicant Total
    15
    Review Days
    85

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    Basic Information

    Device Name
    DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELEC
    K Number
    K850132
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2360
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Consolidated Medical Equipment, Inc.
    Date Received
    January 14, 1985
    Decision Date
    April 9, 1985
    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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