USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 — U.S. Drug Testing, Inc. (510(k) K932318)
USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 — U.S. Drug Testing, Inc. (510(k) K932318) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200; Applicant: U.S. Drug Testing, Inc.; Clearance track: 510(k).
| Device name | USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 |
|---|---|
| Applicant | U.S. Drug Testing, Inc. |
| Clearance track | 510(k) |
| Submission number | K932318 |
| Decision | Substantially Equivalent |
| Decision date | 1993-06-15 |
| Date received | 1993-05-11 |
| Product code | DJG |
| Device class | 2 |
| Medical specialty | Clinical Toxicology |
| Applicant location | CA, US |
| Source | openFDA device |
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