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FDA 510(k) Applications for Medical Device Product Code "NID"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K101911 | CYLEX, INC. | IMMUKNOW-THE CYLEX IMMUNE CELLFUNCTION ASSAY | 10/18/2010 |
K013169 | CYLEX, INC. | IMMUNE CELL FUNCTION ASSAY | 04/02/2002 |