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

    LIQUIBAND DENTAL

    K Number: K993556 · Decision Jan 3, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    144
    Registration Numbers
    144
    Same Product Code
    504
    Applicant Total
    2
    Review Days
    75

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    Basic Information

    Device Name
    LIQUIBAND DENTAL
    K Number
    K993556
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3275
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medlogic Global Corp.
    Date Received
    October 20, 1999
    Decision Date
    January 3, 2000
    Product Code
    EMA
    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
    EMA Cement, Dental

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    Other Clearances by Medlogic Global Corp.

    K Number Device Name
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