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

    STERILE AMBULATORY RESERVOIR 60ML/100ML

    K Number: K962159 · Decision Jul 18, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    37
    Registration Numbers
    37
    Same Product Code
    47
    Applicant Total
    6
    Review Days
    409

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    Basic Information

    Device Name
    STERILE AMBULATORY RESERVOIR 60ML/100ML
    K Number
    K962159
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Faulding Medical Device Co.
    Date Received
    June 4, 1996
    Decision Date
    July 18, 1997
    Product Code
    MRZ
    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
    MRZ Accessories, Pump, Infusion

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