BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

    PADS MENSTRUAL, UNTREAT DEODORIZED, VARIOUS SIZES

    K Number: K933879 · Decision Mar 24, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    307
    Registration Numbers
    307
    Same Product Code
    135
    Applicant Total
    2
    Review Days
    227

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    Basic Information

    Device Name
    PADS MENSTRUAL, UNTREAT DEODORIZED, VARIOUS SIZES
    K Number
    K933879
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    884.5435
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Universal Health Care Products Canada, Inc.
    Date Received
    August 9, 1993
    Decision Date
    March 24, 1994
    Product Code
    HHD
    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
    HHD Pad, Menstrual, Unscented

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    Other Clearances by Universal Health Care Products Canada, Inc.

    K Number Device Name
    K875309 SANITARY MENSTRUAL NAPKIN