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

    IMPEDANCE RHEOGRAPH

    K Number: K772093 · Decision Nov 18, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    2
    Applicant Total
    2
    Review Days
    11

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    Basic Information

    Device Name
    IMPEDANCE RHEOGRAPH
    K Number
    K772093
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2750
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Dynatech Research & Development Co.
    Date Received
    November 7, 1977
    Decision Date
    November 18, 1977
    Product Code
    DQB
    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
    DQB Phlebograph, Impedance

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