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

    SCIMED ENCORE ADVANTAGE KIT AND THE ESSENTIALS KIT

    K Number: K951802 · Decision Jul 21, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    209
    Applicant Total
    109
    Review Days
    93

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    Basic Information

    Device Name
    SCIMED ENCORE ADVANTAGE KIT AND THE ESSENTIALS KIT
    K Number
    K951802
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1650
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Scimed Life Systems, Inc.
    Date Received
    April 19, 1995
    Decision Date
    July 21, 1995
    Product Code
    DXT
    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
    DXT Injector And Syringe, Angiographic

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