K902579 is an FDA 510(k) clearance for the EMIT(R) II COCAINE METABOLITE ASSAY. This device is classified as a Enzyme Immunoassay, Cocaine And Cocaine Metabolites (Class II - Special Controls, product code DIO).
Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on July 27, 1990, 46 days after receiving the submission on June 11, 1990.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3250.
| 510(k) Number | K902579 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 11, 1990 |
| Decision Date | July 27, 1990 |
| Days to Decision | 46 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | DIO — Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3250 |