FDA 510(K) K244027, SANSA HSAT

FDA 510(K) K244027, SANSA HSAT

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Device Classification Name    Ventilatory Effort Recorder
510(k) Number    K244027
Device Name    SANSA HSAT
Applicant    Huxley Medical
Regulation Number    868.2375
Classification Product Code    MNR  
Subsequent Product Code    BZQ  
Date Received    12/30/2024
Decision Date    01/28/2025
Decision    Substantially Equivalent (SESE)
Regulation Medical Specialty    Anesthesiology
510k Review Panel    Anesthesiology
Type    Special
Reviewed by Third Party    No
Combination Product    No

Total pages: 771
Fully redacted pages: 514
Content pages: 257

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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