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

    BD GENEOHM MRSA ACP ASSAY

    K Number: K093346 · Decision Dec 15, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    23
    Applicant Total
    2
    Review Days
    50

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    Basic Information

    Device Name
    BD GENEOHM MRSA ACP ASSAY
    K Number
    K093346
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1640
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bd Diagnostics (Geneohm Sciences, Inc.)
    Date Received
    October 26, 2009
    Decision Date
    December 15, 2009
    Product Code
    NQX
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen

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    Other Clearances by Bd Diagnostics (Geneohm Sciences, Inc.)

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