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

    GLOBE RES-Q-FLO

    K Number: K834128 · Decision Dec 29, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    30

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    Basic Information

    Device Name
    GLOBE RES-Q-FLO
    K Number
    K834128
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Globe Safety Equipment, Inc.
    Date Received
    November 29, 1983
    Decision Date
    December 29, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N