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

    LIGHT SABER SPINAL NEEDLE

    K Number: K021084 · Decision Jul 3, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    14
    Review Days
    90

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    Basic Information

    Device Name
    LIGHT SABER SPINAL NEEDLE
    K Number
    K021084
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Minrad, Inc.
    Date Received
    April 4, 2002
    Decision Date
    July 3, 2002
    Product Code
    FMF
    Advisory Committee
    General Hospital
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FMF Syringe, Piston

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