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    FDA 510(k), K863815, ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000

    FDA 510(k), K863815, ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000

    $89.00 USD
    $89.00 USD
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    510(K) Number: K863815
    Device Name: ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
    Manufacturer:
    Device Classification Name: Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
    Regulation Number: 882.5940
    Classification Product Code: QGH
    Date Received: 09/30/1986
    Decision Date: 06/02/1987
    Regulation Medical Specialty: Neurology

    PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.

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