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

    DRG QUICKMIX

    K Number: K011736 · Decision Jan 30, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    43
    Applicant Total
    13
    Review Days
    239

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    Basic Information

    Device Name
    DRG QUICKMIX
    K Number
    K011736
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5300
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Doctor'S Research Group, Inc.
    Date Received
    June 5, 2001
    Decision Date
    January 30, 2002
    Product Code
    GXP
    Advisory Committee
    Neurology
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GXP Methyl Methacrylate For Cranioplasty

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