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    FDA 510(k), K062187, BETACHEK GLUCOSE TEST

    FDA 510(k), K062187, BETACHEK GLUCOSE TEST

    $89.00 USD
    $89.00 USD
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    510(K) Number: K062187
    Device Name: BETACHEK GLUCOSE TEST
    Manufacturer:
    Device Classification Name: System, Test, Blood Glucose, Over The Counter
    Regulation Number: 862.1345
    Classification Product Code: NBW
    Date Received: 08/01/2006
    Decision Date: 03/24/2009
    Regulation Medical Specialty: Clinical Chemistry

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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