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

    BAXTER DUPLOSPRAY MIS APPLICATOR

    K Number: K061092 · Decision Sep 13, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    29
    Review Days
    147

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    Basic Information

    Device Name
    BAXTER DUPLOSPRAY MIS APPLICATOR
    K Number
    K061092
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Micromedics, Inc.
    Date Received
    April 19, 2006
    Decision Date
    September 13, 2006
    Product Code
    FMF
    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
    FMF Syringe, Piston

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