K931536 is an FDA 510(k) clearance for the EMIT(R) D.A.U. BENZODIAZEPINE ASSAY. This device is classified as a Enzyme Immunoassay, Benzodiazepine (Class II - Special Controls, product code JXM).
Submitted by Syva Co. (San Jose, US). The FDA issued a Cleared decision on May 11, 1993, 43 days after receiving the submission on March 29, 1993.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3170.
| 510(k) Number | K931536 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 29, 1993 |
| Decision Date | May 11, 1993 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | JXM — Enzyme Immunoassay, Benzodiazepine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3170 |