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

    REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION

    K Number: K931595 · Decision Dec 29, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    61
    Registration Numbers
    61
    Same Product Code
    116
    Applicant Total
    1
    Review Days
    638

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    Basic Information

    Device Name
    REVERSE OSMOSIS EQUIPMENT FOR WATER PURIFICATION
    K Number
    K931595
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5665
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Osmonics, Inc.
    Date Received
    March 31, 1993
    Decision Date
    December 29, 1994
    Product Code
    FIP
    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
    FIP Subsystem, Water Purification

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