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

    MINNILERT(R) PRESSURE MONITOR

    K Number: K913483 · Decision Sep 27, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    49
    Registration Numbers
    49
    Same Product Code
    181
    Applicant Total
    33
    Review Days
    52

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    Basic Information

    Device Name
    MINNILERT(R) PRESSURE MONITOR
    K Number
    K913483
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Minntech Corp.
    Date Received
    August 6, 1991
    Decision Date
    September 27, 1991
    Product Code
    KOC
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KOC Accessories, Blood Circuit, Hemodialysis

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    K050952 HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR
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