BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    PERI-GUARD PERICARDIAL PATCH-HERNIA

    K Number: K833021 · Decision Dec 26, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    89
    Applicant Total
    1
    Review Days
    111

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    Basic Information

    Device Name
    PERI-GUARD PERICARDIAL PATCH-HERNIA
    K Number
    K833021
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.3470
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Genetic
    Date Received
    September 6, 1983
    Decision Date
    December 26, 1983
    Product Code
    DXZ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

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