BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇲🇽 Mexico

    VEN-O-VAC BLOOD COLLECTION VACUUM TUBES

    K Number: K900856 · Decision Sep 21, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    218
    Registration Numbers
    218
    Same Product Code
    235
    Applicant Total
    1
    Review Days
    210

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    Basic Information

    Device Name
    VEN-O-VAC BLOOD COLLECTION VACUUM TUBES
    K Number
    K900856
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1675
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Artefactos DE Vidrio S.A. DE C.V.
    Date Received
    February 23, 1990
    Decision Date
    September 21, 1990
    Product Code
    JKA
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

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