DGQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Whole Blood Plasma, Antigen, Antiserum, Control
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.5700
- Medical specialty
- Immunology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ANTI-HUMAN SERUM (K791282) | Diagnostica, Inc. | 1979-10-17 |
Track DGQ automatically
Every clearance here is in the API, with alerts when new ones post.