FDA 510K (K140665) GenPrime Snap-Top Split Key Cup

FDA 510K (K140665) GenPrime Snap-Top Split Key Cup

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Device Classification Name    Enzyme Immunoassay, Barbiturate
510(k) Number    K140665
Device Name    GenPrime Snap-Top Split Key Cup
Applicant    GENPRIME, INC
Regulation Number    862.3150
Classification Product Code    DIS  
Subsequent Product Codes    DIO      JXM  
Date Received    03/18/2014
Decision Date    12/08/2014
Decision    Substantially Equivalent (SESE)
Regulation Medical Specialty    Toxicology

Total pages: 542
Fully redacted pages: 452
Content pages: 90

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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