Submission Details
| 510(k) Number | K940912 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 25, 1994 |
| Decision Date | June 02, 1994 |
| Days to Decision | 97 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
K940912 is an FDA 510(k) clearance for the USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500, a Enzyme Immunoassay, Cannabinoids (Class II — Special Controls, product code LDJ), submitted by U.S. Drug Testing, Inc. (Rancho Cucamonga, US). The FDA issued a Cleared decision on June 2, 1994, 97 days after receiving the submission on February 25, 1994. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3870.
| 510(k) Number | K940912 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 25, 1994 |
| Decision Date | June 02, 1994 |
| Days to Decision | 97 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
| Product Code | LDJ — Enzyme Immunoassay, Cannabinoids |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.3870 |