BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT

    K Number: K973176 · Decision Nov 21, 1997
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    88

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    Basic Information

    Device Name
    SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT
    K Number
    K973176
    Clearance Type
    Traditional
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Lotus Technologies
    Date Received
    August 25, 1997
    Decision Date
    November 21, 1997
    Product Code
    KGA
    Advisory Committee
    Unknown
    Review Advisory Committee
    AN
    Third Party
    N