DLT
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hemagglutination, Opiates
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3650
- Medical specialty
- Clinical Toxicology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| URINE NEGATIVE CALIBRATOR (K790400) | Syva Co. | 1979-06-15 |
Track DLT automatically
Every clearance here is in the API, with alerts when new ones post.