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

    PRO-KUP

    K Number: K770556 · Decision Mar 24, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    116
    Registration Numbers
    116
    Same Product Code
    7
    Applicant Total
    1
    Review Days
    3

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    Basic Information

    Device Name
    PRO-KUP
    K Number
    K770556
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6290
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Dental Control Products
    Date Received
    March 21, 1977
    Decision Date
    March 24, 1977
    Product Code
    EHK
    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
    EHK Cup, Prophylaxis

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