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

    GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE

    K Number: K913696 · Decision Feb 18, 1992
    View on FDA
    Classifications
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    80
    Applicant Total
    1
    Review Days
    183

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    Basic Information

    Device Name
    GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE
    K Number
    K913696
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Vertex Technical Group, Inc.
    Date Received
    August 19, 1991
    Decision Date
    February 18, 1992
    Product Code
    LDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

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