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

    CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS

    K Number: K091964 · Decision Sep 24, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    335
    Registration Numbers
    336
    Same Product Code
    61
    Applicant Total
    23
    Review Days
    85

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    Basic Information

    Device Name
    CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS
    K Number
    K091964
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6390
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Procter & Gamble Co.
    Date Received
    July 1, 2009
    Decision Date
    September 24, 2009
    Product Code
    JES
    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
    JES Floss, Dental

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