BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER

    K Number: K896481 · Decision May 15, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    14
    Registration Numbers
    14
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    181

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    Basic Information

    Device Name
    PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER
    K Number
    K896481
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6855
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Purebrush Assoc.
    Date Received
    November 15, 1989
    Decision Date
    May 15, 1990
    Product Code
    MCF
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MCF Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile

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