FDA 510(K), K152768 Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip

FDA 510(K), K152768 Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip

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Device Classification Name    Visual, Pregnancy Hcg, Prescription Use
510(k) Number    K152768
Device Name    Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip
Applicant    ASSURE TECH. CO., LTD.
Regulation Number    862.1155
Classification Product Code    JHI  
Date Received    09/24/2015
Decision Date    02/24/2016
Decision    Substantially Equivalent (SESE)
Regulation Medical Specialty    Clinical Chemistry

Total pages: 349
Fully redacted pages: 234
Content pages: 115

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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