FDA 510(K) K244027, SANSA HSAT
FDA 510(K) K244027, SANSA HSAT
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
Couldn't load pickup availability
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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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.
View full details