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

    CUFFCHECK

    K Number: K881178 · Decision Apr 14, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    38
    Applicant Total
    43
    Review Days
    27

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    Basic Information

    Device Name
    CUFFCHECK
    K Number
    K881178
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5750
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Dhd Medical Products Div. Diemolding Corp.
    Date Received
    March 18, 1988
    Decision Date
    April 14, 1988
    Product Code
    BSK
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    BSK Cuff, Tracheal Tube, Inflatable

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    Other Clearances by Dhd Medical Products Div. Diemolding Corp.

    K Number Device Name
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    K874047 ASTHMAKIT
    K873447 DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR
    K860873 VENTURI MASK/ADULT & PAEDIATRIC
    K860879 DISPOSABLE VENTILATOR CIRCUITS
    K860880 VENTILATOR CIRCUITS (VARIOUS TYPES)
    K860878 BRITISH BREATHING CIRCUIT SYSTEM
    K860877 FLEXTUBE, CONNECTING TUBING
    Search all 43 clearances from Dhd Medical Products Div. Diemolding Corp. →