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

    ACCU-PAQUE

    K Number: K771886 · Decision Nov 14, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    158
    Registration Numbers
    158
    Same Product Code
    481
    Applicant Total
    26
    Review Days
    40

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    Basic Information

    Device Name
    ACCU-PAQUE
    K Number
    K771886
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.6660
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Williams Gold Refining Co., Inc.
    Date Received
    October 5, 1977
    Decision Date
    November 14, 1977
    Product Code
    EIH
    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
    EIH Powder, Porcelain

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    K844394 RENAISSANCE BONDING AGENT
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