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

    BBL ANAGEL POWDER

    K Number: K832229 · Decision Aug 12, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    17
    Applicant Total
    632
    Review Days
    32

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    Basic Information

    Device Name
    BBL ANAGEL POWDER
    K Number
    K832229
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2580
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Bd Becton Dickinson Vacutainer Systems Preanalytic
    Date Received
    July 11, 1983
    Decision Date
    August 12, 1983
    Product Code
    KZJ
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KZJ Device, Gas Generating

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