K020771 is an FDA 510(k) clearance for the ACON ONE STEP DRUG SCREEN TEST CARD. This device is classified as a Enzyme Immunoassay, Cocaine And Cocaine Metabolites (Class II - Special Controls, product code DIO).
Submitted by ACON Laboratories, Inc. (San Diego, US). The FDA issued a Cleared decision on May 15, 2002, 68 days after receiving the submission on March 8, 2002.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3250.
| 510(k) Number | K020771 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 08, 2002 |
| Decision Date | May 15, 2002 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | DIO — Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3250 |