BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    CARDIFF ALDASORBER SYSTEM

    K Number: K811703 · Decision Jun 16, 1981
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    —

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    Basic Information

    Device Name
    CARDIFF ALDASORBER SYSTEM
    K Number
    K811703
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    William Harvey Life Products Corp.
    Date Received
    June 16, 1981
    Decision Date
    June 16, 1981
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

    Other Clearances by William Harvey Life Products Corp.

    K Number Device Name
    K810065 SCOTT CM42 PASTEURIZER
    K770720 TUBING PACK, EXTRACORPOREAL, H-3000