BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

    STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUS

    K Number: K972030 · Decision Sep 8, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    19
    Applicant Total
    36
    Review Days
    98

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    Basic Information

    Device Name
    STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUS
    K Number
    K972030
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2660
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Oxoid , Ltd.
    Date Received
    June 2, 1997
    Decision Date
    September 8, 1997
    Product Code
    JWX
    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
    JWX Kit, Screening, Staphylococcus Aureus

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