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    FDA 510(k), K991543, INTRAOP CATHETER

    FDA 510(k), K991543, INTRAOP CATHETER

    $89.00 USD
    $89.00 USD
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    510(K) Number: K991543
    Device Name: INTRAOP CATHETER
    Manufacturer:
    Device Classification Name: Pump, Infusion, Elastomeric
    Regulation Number: 880.5725
    Classification Product Code: MEB
    Date Received: 05/03/1999
    Decision Date: 10/25/1999
    Regulation Medical Specialty: General Hospital

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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