BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    PULLEN POCKET SCOPE

    K Number: K802818 · Decision Apr 17, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    50
    Registration Numbers
    50
    Same Product Code
    8
    Applicant Total
    2
    Review Days
    161

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    Basic Information

    Device Name
    PULLEN POCKET SCOPE
    K Number
    K802818
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    864.3600
    Medical Specialty
    Pathology
    Decision
    Substantially Equivalent
    Applicant
    P.A. Research Corp.
    Date Received
    November 7, 1980
    Decision Date
    April 17, 1981
    Product Code
    IBJ
    Advisory Committee
    Pathology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IBJ Light, Microscope

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