Submission Details
| 510(k) Number | K983703 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 21, 1998 |
| Decision Date | December 11, 1998 |
| Days to Decision | 51 days |
| Submission Type | Special |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
K983703 is an FDA 510(k) clearance for the MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE, a Enzyme Immunoassay, Methadone (Class II — Special Controls, product code DJR), submitted by Roche Diagnostic Systems, Inc. (Somerville, US). The FDA issued a Cleared decision on December 11, 1998, 51 days after receiving the submission on October 21, 1998. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3620.
| 510(k) Number | K983703 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 21, 1998 |
| Decision Date | December 11, 1998 |
| Days to Decision | 51 days |
| Submission Type | Special |
| Review Panel | Toxicology (TX) |
| Summary | Summary PDF |
| Product Code | DJR — Enzyme Immunoassay, Methadone |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.3620 |