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

    I BRADYKININ & ANTI-BRADYKININ ANTISERUM

    K Number: K790362 · Decision Apr 23, 1979
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    5
    Review Days
    60

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    Basic Information

    Device Name
    I BRADYKININ & ANTI-BRADYKININ ANTISERUM
    K Number
    K790362
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Cambridge Nuclear Corp.
    Date Received
    February 22, 1979
    Decision Date
    April 23, 1979
    Advisory Committee
    Unknown
    Review Advisory Committee
    IM
    Third Party
    N

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    K790008 I ESTRIOL