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

    DISPOSABLE CONTROLLED DROP PASTEUR PIPET

    K Number: K780237 · Decision Mar 9, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    24

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    Basic Information

    Device Name
    DISPOSABLE CONTROLLED DROP PASTEUR PIPET
    K Number
    K780237
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    864.6160
    Medical Specialty
    Hematology
    Decision
    Substantially Equivalent
    Applicant
    Owens-Illinois, Inc.
    Date Received
    February 13, 1978
    Decision Date
    March 9, 1978
    Product Code
    GJG
    Advisory Committee
    Hematology
    Review Advisory Committee
    HE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GJG Pipette, Quantitative, Hematology

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