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

    MYLAB30, MODEL 7300

    K Number: K071996 · Decision Aug 3, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    348
    Registration Numbers
    349
    Same Product Code
    892
    Applicant Total
    67
    Review Days
    8

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    Basic Information

    Device Name
    MYLAB30, MODEL 7300
    K Number
    K071996
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1560
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Esaote, S.p.A.
    Date Received
    July 26, 2007
    Decision Date
    August 3, 2007
    Product Code
    IYO
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    IYO System, Imaging, Pulsed Echo, Ultrasonic

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    Other Clearances by Esaote, S.p.A.

    K Number Device Name
    K253288 6450 Ultrasound System (MyLabE80); 6450 Ultrasound System (MyLabE85)
    K260746 S-scan Open (100001800)
    K251901 Magnifico Open (100009900)
    K253310 7600 Ultrasound System (MyLabC25); 7600 Ultrasound System (MyLabC30)
    K243253 6600 Ultrasound System (MyLabA50); 6600 Ultrasound System (MyLabA70)
    K241671 6450 Ultrasound System (MyLabE80); 6450 Ultrasound System (MyLabE85)
    K241133 Magnifico Open (100009900); Magnifico MSK ( 100009910)
    K230179 6440 MyLabX90
    K212419 Magnifico Open, Magnifico MSK
    K212021 6430 MyLabX75, 6430 MyLab XPro75
    Search all 67 clearances from Esaote, S.p.A. →