K780461 is an FDA 510(k) clearance for the ANALYZER-SUPPLEMENT, KINETIC, LKB 2086. 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 April 12, 1978, 20 days after receiving the submission on March 23, 1978.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3380.
| 510(k) Number | K780461 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 23, 1978 |
| Decision Date | April 12, 1978 |
| Days to Decision | 20 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 |