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    FDA 510(k), K930622, AMPLATZ GUIDEWIRES

    FDA 510(k), K930622, AMPLATZ GUIDEWIRES

    $89.00 USD
    $89.00 USD
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    510(K) Number: K930622
    Device Name: AMPLATZ GUIDEWIRES
    Manufacturer:
    Device Classification Name: Wire, Guide, Catheter
    Regulation Number: 870.1330
    Classification Product Code: DQX
    Date Received: 02/08/1993
    Decision Date: 04/29/1993
    Regulation Medical Specialty: Cardiovascular

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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