K802621 is an FDA 510(k) clearance for the EMIT-STM ETHYL ALCOHOL ASSAY. This device is classified as a Enzymatic Method, Alcohol Dehydrogenase, Ultraviolet (Class II - Special Controls, product code DMT).
Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on October 31, 1980, 11 days after receiving the submission on October 20, 1980.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3040.
| 510(k) Number | K802621 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 20, 1980 |
| Decision Date | October 31, 1980 |
| Days to Decision | 11 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | DMT — Enzymatic Method, Alcohol Dehydrogenase, Ultraviolet |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3040 |