K012131 is an FDA 510(k) clearance for the LIVESURE BENZODIAZEPINES SCREEN TESTS. This device is classified as a Enzyme Immunoassay, Benzodiazepine (Class II - Special Controls, product code JXM).
Submitted by Pan Probe Biotech, Inc. (San Diego, US). The FDA issued a Cleared decision on July 20, 2001, 11 days after receiving the submission on July 9, 2001.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3170.
| 510(k) Number | K012131 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 09, 2001 |
| Decision Date | July 20, 2001 |
| Days to Decision | 11 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | JXM — Enzyme Immunoassay, Benzodiazepine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3170 |