K170222 is an FDA 510(k) clearance for the Rapid Tox Cup II. This device is classified as a Gas Chromatography, Methamphetamine (Class II - Special Controls, product code LAF).
Submitted by American Bio Medica Corp. (Kinderhook, US). The FDA issued a Cleared decision on August 15, 2017, 202 days after receiving the submission on January 25, 2017.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3610.
| 510(k) Number | K170222 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 25, 2017 |
| Decision Date | August 15, 2017 |
| Days to Decision | 202 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 |