Submission Details
| 510(k) Number | K002268 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 25, 2000 |
| Decision Date | November 27, 2000 |
| Days to Decision | 125 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
K002268 is an FDA 510(k) clearance for the BRANAN MEDICAL CORPORATION MONITECT MORPHINE 2000 DRUG SCREEN TEST, a Enzyme Immunoassay, Opiates (Class II — Special Controls, product code DJG), submitted by Branan Medical Corporation (Irvine, US). The FDA issued a Cleared decision on November 27, 2000, 125 days after receiving the submission on July 25, 2000. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3650.
| 510(k) Number | K002268 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 25, 2000 |
| Decision Date | November 27, 2000 |
| Days to Decision | 125 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
| Product Code | DJG — Enzyme Immunoassay, Opiates |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.3650 |