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

    CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM

    K Number: K933151 · Decision Dec 13, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    194
    Registration Numbers
    194
    Same Product Code
    321
    Applicant Total
    18
    Review Days
    167

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    Basic Information

    Device Name
    CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM
    K Number
    K933151
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6850
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Contour Fabricators of Florida, Inc.
    Date Received
    June 29, 1993
    Decision Date
    December 13, 1993
    Product Code
    FRG
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FRG Wrap, Sterilization

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