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

    TUBE HOLDER

    K Number: K801421 · Decision Jul 28, 1980
    View on FDA
    Classifications
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    80
    Applicant Total
    47
    Review Days
    41

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    Basic Information

    Device Name
    TUBE HOLDER
    K Number
    K801421
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Devon Industries, Inc.
    Date Received
    June 17, 1980
    Decision Date
    July 28, 1980
    Product Code
    LDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

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