K820188 is an FDA 510(k) clearance for the PHENOBARBITAL ASSAY. This device is classified as a Fluorescent Immunoassay, Phenobarbital (Class II - Special Controls, product code LET).
Submitted by Syva Co. (Walker, US). The FDA issued a Cleared decision on February 5, 1982, 11 days after receiving the submission on January 25, 1982.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3660.
| 510(k) Number | K820188 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 25, 1982 |
| Decision Date | February 05, 1982 |
| Days to Decision | 11 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | LET — Fluorescent Immunoassay, Phenobarbital |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3660 |