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

    VENES CUSTON RX

    K Number: K820484 · Decision Mar 18, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    268
    Registration Numbers
    268
    Same Product Code
    5
    Applicant Total
    2
    Review Days
    24

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    Basic Information

    Device Name
    VENES CUSTON RX
    K Number
    K820484
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5780
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Jung Products, Inc.
    Date Received
    February 22, 1982
    Decision Date
    March 18, 1982
    Product Code
    FQL
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FQL Stocking, Medical Support (For General Medical Purposes)

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    Other Clearances by Jung Products, Inc.

    K Number Device Name
    K811085 VENES II