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

    IDEAS' PORT

    K Number: K913602 · Decision Jan 2, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    16
    Review Days
    142

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    Basic Information

    Device Name
    IDEAS' PORT
    K Number
    K913602
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Ideal Medical, Inc.
    Date Received
    August 13, 1991
    Decision Date
    January 2, 1992
    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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    Other Clearances by Ideal Medical, Inc.

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    K922161 GRICE SOFT TISSUE BIOPSY KIT
    K921922 GRICE LAPAROSCOPIC SUTURING NEEDLE
    K915175 REDDICK RETRACTOR
    K914880 DUAL BALLOON EMBOLECTOMY CATHETER
    K914913 GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST
    K912540 CONTOUR-PORT
    K911601 REDDICK TROCAR AND CANNULA
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