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

    MICROSPAN HYSTEROSCOPE SHEATH

    K Number: K961506 · Decision Jul 3, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    135
    Registration Numbers
    135
    Same Product Code
    170
    Applicant Total
    19
    Review Days
    75

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    Basic Information

    Device Name
    MICROSPAN HYSTEROSCOPE SHEATH
    K Number
    K961506
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1690
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Imagyn Medical, Inc.
    Date Received
    April 19, 1996
    Decision Date
    July 3, 1996
    Product Code
    HIH
    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
    HIH Hysteroscope (And Accessories)

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    Other Clearances by Imagyn Medical, Inc.

    K Number Device Name
    K972426 MICROSPAN GOLD HYSTEROSCOPE AND MICROSPAN HYSTEROSCOPE SHEATH
    K970750 MICROSPAN INSEMINATION SYSTEM
    K971255 IMAGYN EXPANDABLE LAPAROSCOPIC INTRODUCER
    K965055 IMAGYN MICROLAP AND MICRO LAP-GOLD LAPAROSCOPES
    K963580 IMAGYN FALLOPOSCOPY SYSTEM
    K961688 MICROSPAN HYSTEROSCOPE
    K952032 IMAGYN HYSTEROSCOPE SHEATHS
    K951996 IMAGYN ENDOSCOPE
    K951974 IMAGYN ENDOSCOPE SHEATH
    K953201 IMAGYN UROSCOPE
    Search all 19 clearances from Imagyn Medical, Inc. →