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

    ECG TELEMETRY SYSTEM

    K Number: K772000 · Decision Nov 22, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    125
    Registration Numbers
    125
    Same Product Code
    190
    Applicant Total
    6
    Review Days
    32

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    Basic Information

    Device Name
    ECG TELEMETRY SYSTEM
    K Number
    K772000
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2910
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Mennen Greatbatch Electonics
    Date Received
    October 21, 1977
    Decision Date
    November 22, 1977
    Product Code
    DRG
    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
    DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

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