DLR
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hemagglutination Inhibition, Morphine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3640
- 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 |
|---|---|---|
| HI-M-TEST MORPHINE (K791551) | Technam, Inc. | 1979-10-17 |
| KIT, MORPHINE (TOXI-PAK IMMUNO HI) (K760074) | J.T. Baker Chemical Co. | 1976-07-20 |
Track DLR automatically
Every clearance here is in the API, with alerts when new ones post.