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

    INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION

    K Number: K880208 · Decision Apr 12, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59
    Same Product Code
    270
    Applicant Total
    2
    Review Days
    88

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    Basic Information

    Device Name
    INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION
    K Number
    K880208
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Dresser Argus, Inc.
    Date Received
    January 15, 1988
    Decision Date
    April 12, 1988
    Product Code
    EFQ
    Advisory Committee
    Unknown
    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
    EFQ Gauze/Sponge, Internal

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    Other Clearances by Dresser Argus, Inc.

    K Number Device Name
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