BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇰 Denmark

    VACCON

    K Number: K896733 · Decision Feb 1, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    972
    Registration Numbers
    972
    Same Product Code
    186
    Applicant Total
    7
    Review Days
    63

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    Basic Information

    Device Name
    VACCON
    K Number
    K896733
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5240
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Unoplast A/S
    Date Received
    November 30, 1989
    Decision Date
    February 1, 1990
    Product Code
    KGX
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KGX Tape And Bandage, Adhesive

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    Other Clearances by Unoplast A/S

    K Number Device Name
    K896734 FEEDING TUBE
    K896729 NELATON-, FEMALE - OR TIEMANN CATHETER
    K896732 UNOMETER 500
    K896731 OXYGEN CATHETERS
    K896730 SUCTION CATHETER STRAIGHT/COUDE
    K802248 DISARP ORIGINAL