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

    VACUETTE MULTIPLE SAMPLE LUER ADAPTER

    K Number: K981619 · Decision Jul 15, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    440
    Registration Numbers
    440
    Same Product Code
    687
    Applicant Total
    10
    Review Days
    70

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    Basic Information

    Device Name
    VACUETTE MULTIPLE SAMPLE LUER ADAPTER
    K Number
    K981619
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5570
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Greiner Meditech, Inc.
    Date Received
    May 6, 1998
    Decision Date
    July 15, 1998
    Product Code
    FMI
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FMI Needle, Hypodermic, Single Lumen

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