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

    ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA

    K Number: K936155 · Decision Apr 11, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    176
    Applicant Total
    7
    Review Days
    105

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    Basic Information

    Device Name
    ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA
    K Number
    K936155
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1730
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Micromedical Devices, Inc.
    Date Received
    December 27, 1993
    Decision Date
    April 11, 1994
    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 Micromedical Devices, Inc.

    K Number Device Name
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    K936195 LAPAROSCOPES
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    K936086 STERILE VIDEO CAMERA COVER AND DRAPE
    K850791 MDI 2000 - PULSE GENERATOR
    K834262 TRANS-PACE