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    FDA 510(k), K210635, Route 92 Medical Full Length 088 Access System

    FDA 510(k), K210635, Route 92 Medical Full Length 088 Access System

    $89.00 USD
    $89.00 USD
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    510(K) Number: K210635
    Device Name: Route 92 Medical Full Length 088 Access System
    Manufacturer: Kirsten Valley
    Device Classification Name: Catheter, Percutaneous, Neurovasculature
    Regulation Number: QJP
    Classification Product Code: KXA
    Date Received: 03/03/2021
    Decision Date: 07/27/2021
    Decision: Substantially Equivalent (SESE)
    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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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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