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

    SIEMENS SI-400

    K Number: K914013 · Decision Dec 2, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    348
    Registration Numbers
    349
    Same Product Code
    892
    Applicant Total
    8
    Review Days
    84

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    Basic Information

    Device Name
    SIEMENS SI-400
    K Number
    K914013
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1560
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Siemens Ultrasound, Inc.
    Date Received
    September 9, 1991
    Decision Date
    December 2, 1991
    Product Code
    IYO
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    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 Siemens Ultrasound, Inc.

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    K910529 7.5 MHZ PEDIATRIC TRANSESOPHAGEAL ECHO (TEE) TRANS
    K910669 5 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU
    K891449 SONOLINE CF
    K891238 SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER