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    FDA 510(k), K024322, EMBLA N7000

    FDA 510(k), K024322, EMBLA N7000

    $89.00 USD
    $89.00 USD
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    510(K) Number: K024322
    Device Name: EMBLA N7000
    Manufacturer:
    Device Classification Name: Ventilatory Effort Recorder
    Regulation Number: 868.2375
    Classification Product Code: MNR
    Date Received: 12/26/2002
    Decision Date: 10/27/2003
    Regulation Medical Specialty: Anesthesiology

    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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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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