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

    MINRAD DRTS LIGHT SABER SYRINGE

    K Number: K981140 · Decision Jun 25, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    14
    Review Days
    87

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    Basic Information

    Device Name
    MINRAD DRTS LIGHT SABER SYRINGE
    K Number
    K981140
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Minrad, Inc.
    Date Received
    March 30, 1998
    Decision Date
    June 25, 1998
    Product Code
    FMF
    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
    FMF Syringe, Piston

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