K093884 is an FDA 510(k) clearance for the ROCHE FLUDI METHAMPHETAMINE. This device is classified as a Gas Chromatography, Methamphetamine (Class II - Special Controls, product code LAF).
Submitted by Roche Diagnostics (Indianapolis, US). The FDA issued a Cleared decision on February 25, 2011, 434 days after receiving the submission on December 18, 2009.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3610.
| 510(k) Number | K093884 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 18, 2009 |
| Decision Date | February 25, 2011 |
| Days to Decision | 434 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | LAF — Gas Chromatography, Methamphetamine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3610 |