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    FDA 510(k), K063626, DURAFLEX

    FDA 510(k), K063626, DURAFLEX

    $89.00 USD
    $89.00 USD
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    510(K) Number: K063626
    Device Name: DURAFLEX
    Manufacturer:
    Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
    Regulation Number: 872.3760
    Classification Product Code: EBI
    Date Received: 12/06/2006
    Decision Date: 02/08/2007
    Regulation Medical Specialty: Dental

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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