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

    ENDOLAP INSUFFLATOR TUBING SET

    K Number: K950219 · Decision Mar 23, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    142
    Registration Numbers
    142
    Same Product Code
    174
    Applicant Total
    5
    Review Days
    63

    Basic Information

    Device Name
    ENDOLAP INSUFFLATOR TUBING SET
    K Number
    K950219
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1730
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    ENDOLAP, INC.
    Date Received
    January 19, 1995
    Decision Date
    March 23, 1995
    Product Code
    HIF
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HIF Insufflator, Laparoscopic

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    Other Clearances by ENDOLAP, INC.

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