K832797 is an FDA 510(k) clearance for the MODIFICA- OF EMIT AED ETHOSUXIMIDE ASSAY. This device is classified as a Enzyme Immunoassay, Ethosuximide (Class II - Special Controls, product code DLF).
Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on September 29, 1983, 42 days after receiving the submission on August 18, 1983.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3380.
| 510(k) Number | K832797 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 18, 1983 |
| Decision Date | September 29, 1983 |
| Days to Decision | 42 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | DLF — Enzyme Immunoassay, Ethosuximide |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3380 |