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

    THE WHITE RIVER PORTA-ELEC-BREAST PUMP

    K Number: K850705 · Decision Jul 11, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    243
    Applicant Total
    2
    Review Days
    140

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    Basic Information

    Device Name
    THE WHITE RIVER PORTA-ELEC-BREAST PUMP
    K Number
    K850705
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.5160
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Natural Technologies, Inc.
    Date Received
    February 21, 1985
    Decision Date
    July 11, 1985
    Product Code
    HGX
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HGX Pump, Breast, Powered

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    Other Clearances by Natural Technologies, Inc.

    K Number Device Name
    K952712 WHITE RIVER BATTERY-POWERED BREAST PUMP