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

    PLETHYSMOGRAPH (MDI SYSTEM II)

    K Number: K760504 · Decision Aug 26, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    52
    Applicant Total
    1
    Review Days
    3

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    Basic Information

    Device Name
    PLETHYSMOGRAPH (MDI SYSTEM II)
    K Number
    K760504
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2780
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Marketing Development Intl.
    Date Received
    August 23, 1976
    Decision Date
    August 26, 1976
    Product Code
    JOM
    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
    JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

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