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

    MEGA BITE REGISTRATION - DENTAL BITE REGISTRATION MATERIAL

    K Number: K030776 · Decision May 9, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    401
    Applicant Total
    10
    Review Days
    59

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    Basic Information

    Device Name
    MEGA BITE REGISTRATION - DENTAL BITE REGISTRATION MATERIAL
    K Number
    K030776
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3660
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Discus Dental, Inc.
    Date Received
    March 11, 2003
    Decision Date
    May 9, 2003
    Product Code
    ELW
    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
    ELW Material, Impression

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