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

    FILT-R-ALL BACTERIAL FILTER

    K Number: K896832 · Decision Jan 22, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    201
    Applicant Total
    7
    Review Days
    48

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    Basic Information

    Device Name
    FILT-R-ALL BACTERIAL FILTER
    K Number
    K896832
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5260
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Inhalation Plastics
    Date Received
    December 5, 1989
    Decision Date
    January 22, 1990
    Product Code
    CAH
    Advisory Committee
    Anesthesiology
    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
    CAH Filter, Bacterial, Breathing-Circuit

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    Other Clearances by Inhalation Plastics

    K Number Device Name
    K945565 SPIRO-FLEX
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    K901315 AEROMIST II NEBULIZER
    K900990 FILT-R-ALL BACTERIAL/VIRAL FILTER
    K900594 ANESTHESIA BREATHING CIRCUIT
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