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

    CENTRIFUGES

    K Number: K840768 · Decision May 7, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    163
    Registration Numbers
    163
    Same Product Code
    37
    Applicant Total
    2
    Review Days
    74

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    Basic Information

    Device Name
    CENTRIFUGES
    K Number
    K840768
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2050
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Heraeus-Christ GmbH
    Date Received
    February 23, 1984
    Decision Date
    May 7, 1984
    Product Code
    JQC
    Advisory Committee
    Clinical Chemistry
    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
    JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use

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    Other Clearances by Heraeus-Christ GmbH

    K Number Device Name
    K840767 HAEMOFUGE A. BIOFUGE A. & B