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    FDA 510(k), K203722, RayPilot System

    FDA 510(k), K203722, RayPilot System

    $89.00 USD
    $89.00 USD
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    510(K) Number: K203722
    Device Name: RayPilot System
    Manufacturer: Thomas Lindstrom
    Device Classification Name: Accelerator, Linear, Medical
    Regulation Number: IYE
    Classification Product Code: KXA
    Date Received: 12/21/2020
    Decision Date: 09/02/2021
    Decision: Substantially Equivalent (SESE)
    Regulation Medical Specialty: Radiology

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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