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

    MP-50T DISPOSABLE BREATHING CIRCUIT FILTER

    K Number: K862786 · Decision Aug 1, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    201
    Applicant Total
    49
    Review Days
    9

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    Basic Information

    Device Name
    MP-50T DISPOSABLE BREATHING CIRCUIT FILTER
    K Number
    K862786
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5260
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Medipart Jerry Alexander
    Date Received
    July 23, 1986
    Decision Date
    August 1, 1986
    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 Medipart Jerry Alexander

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    K894138 MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD
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