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

    URESIL ENDOSCOPIC LASER OVERTUBE

    K Number: K901882 · Decision Jul 27, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    3
    Applicant Total
    45
    Review Days
    92

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    Basic Information

    Device Name
    URESIL ENDOSCOPIC LASER OVERTUBE
    K Number
    K901882
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3410
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Uresil Corp.
    Date Received
    April 26, 1990
    Decision Date
    July 27, 1990
    Product Code
    KOQ
    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
    KOQ Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)

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