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

    LIQUISPX LIQUID SALIVA OR UNRINE DRUG OF ABUSE CONTROL

    K Number: K012907 · Decision Sep 28, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    201
    Applicant Total
    1
    Review Days
    30

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    Basic Information

    Device Name
    LIQUISPX LIQUID SALIVA OR UNRINE DRUG OF ABUSE CONTROL
    K Number
    K012907
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.3280
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Clinical Controls
    Date Received
    August 29, 2001
    Decision Date
    September 28, 2001
    Product Code
    DIF
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DIF Drug Mixture Control Materials

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