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

    SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM

    K Number: K091720 · Decision Apr 9, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    266
    Registration Numbers
    266
    Same Product Code
    279
    Applicant Total
    2
    Review Days
    302

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    Basic Information

    Device Name
    SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM
    K Number
    K091720
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6850
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sklar Corp.
    Date Received
    June 11, 2009
    Decision Date
    April 9, 2010
    Product Code
    KCT
    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
    KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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    Other Clearances by Sklar Corp.

    K Number Device Name
    K082479 SKLAR SURGICAL GOWN