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

    ELIMINATOR AIR FILTER

    K Number: K882468 · Decision Aug 29, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    47
    Applicant Total
    6
    Review Days
    75

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    Basic Information

    Device Name
    ELIMINATOR AIR FILTER
    K Number
    K882468
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Apex Medical, Inc.
    Date Received
    June 15, 1988
    Decision Date
    August 29, 1988
    Product Code
    KDQ
    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
    KDQ Bottle, Collection, Vacuum

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