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

    PROCHECK(TM) BLIND PERFORMANCE SPECIMENS

    K Number: K931105 · Decision Apr 21, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    201
    Applicant Total
    6
    Review Days
    49

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    Basic Information

    Device Name
    PROCHECK(TM) BLIND PERFORMANCE SPECIMENS
    K Number
    K931105
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.3280
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Dynagen, Inc.
    Date Received
    March 3, 1993
    Decision Date
    April 21, 1993
    Product Code
    DIF
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    TX
    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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