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

    DENTAL X-RAY BITE BLOCK

    K Number: K890355 · Decision Jun 12, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    7
    Applicant Total
    1
    Review Days
    139

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    Basic Information

    Device Name
    DENTAL X-RAY BITE BLOCK
    K Number
    K890355
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.1905
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Bite-A-Block
    Date Received
    January 24, 1989
    Decision Date
    June 12, 1989
    Product Code
    EGZ
    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
    EGZ Holder, Film, X-Ray

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