K020368 is an FDA 510(k) clearance for the OPIATE ENZYME IMMUNOASSAY, CATALOG # 0020 (500 TESTS KIT). This device is classified as a Enzyme Immunoassay, Opiates (Class II - Special Controls, product code DJG).
Submitted by Lin-Zhi International, Inc. (San Jose, US). The FDA issued a Cleared decision on June 4, 2002, 120 days after receiving the submission on February 4, 2002.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3650.
| 510(k) Number | K020368 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 04, 2002 |
| Decision Date | June 04, 2002 |
| Days to Decision | 120 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | DJG — Enzyme Immunoassay, Opiates |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3650 |