Submission Details
| 510(k) Number | K171403 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 12, 2017 |
| Decision Date | February 02, 2018 |
| Days to Decision | 266 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
K171403 is an FDA 510(k) clearance for the OralTox Oral Fluid Drug Test, a Thin Layer Chromatography, Methamphetamine (Class II — Special Controls, product code DJC), submitted by Premier Biotech, Inc. (Minneapolis, US). The FDA issued a Cleared decision on February 2, 2018, 266 days after receiving the submission on May 12, 2017. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3610.
| 510(k) Number | K171403 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 12, 2017 |
| Decision Date | February 02, 2018 |
| Days to Decision | 266 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | DJC — Thin Layer Chromatography, Methamphetamine |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.3610 |