BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    TEMPLATE AND COUNTER-FIT

    K Number: K081017 · Decision Aug 4, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    401
    Applicant Total
    2
    Review Days
    117

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    Basic Information

    Device Name
    TEMPLATE AND COUNTER-FIT
    K Number
    K081017
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3660
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Clinician'S Choice Dental Products, Inc.
    Date Received
    April 9, 2008
    Decision Date
    August 4, 2008
    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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    Other Clearances by Clinician'S Choice Dental Products, Inc.

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