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

    MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

    K Number: K900731 · Decision Dec 17, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    14
    Applicant Total
    6
    Review Days
    305

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    Basic Information

    Device Name
    MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)
    K Number
    K900731
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Medical Consultants Intl. , Ltd.
    Date Received
    February 15, 1990
    Decision Date
    December 17, 1990
    Product Code
    LWM
    Advisory Committee
    Unknown
    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
    LWM Device, Electrical Dental Anesthesia

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    3M DENTAL ELECTRONONIC ANESTHESIA (DEA0 SYSTEM 8670 ADDITIONAL APPLICATIONS

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    Other Clearances by Medical Consultants Intl. , Ltd.

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    K894515 LISS CRANIAL STIMULATOR MODEL SBL201-M
    K896226 LISS BODY STIMULATOR MODEL SBL501-M