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

    PADS, MINI, MAXI DEODORANT

    K Number: K782111 · Decision Jan 8, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    56
    Applicant Total
    10
    Review Days
    21

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    Basic Information

    Device Name
    PADS, MINI, MAXI DEODORANT
    K Number
    K782111
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.5425
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Intl. Playtex, Inc.
    Date Received
    December 18, 1978
    Decision Date
    January 8, 1979
    Product Code
    HHL
    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
    HHL Pad, Menstrual, Scented, Scented-Deodorized

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (HHL), ordered by most recent decision date.

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    ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD

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    FDA Class 2 ·Obstetrics/Gynecology
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    Other Clearances by Intl. Playtex, Inc.

    K Number Device Name
    K871197 PLAYTEX TAMPONS AND DEODORANT TAMPONS
    K861738 PLAYTEX TAMPONS
    K854258 PLAYTEX LIGHT'N GENTLE UNSCENTED/DEODORANT/MINI TA
    K852063 PLAYTEX SLENDER REG. TAMPONS & DEODORANT TAMPONS
    K851356 PLAYTEX SUPER TAMPONS & SUPER DEODORANT TAMPONS
    K851355 PLAYTEX SUPER PLUS TAMPONS & DEODORANT TAMPONS
    K782112 PADS, MINI, MAXI
    K760425 TAMPON, PLAYTEX 2 VERSION A
    K760426 TAMPON, PLAYTEX 2 VERSION B