GNH
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antigen, Fluorescent Antibody Test, Schistosoma Mansoni
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3600
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ANTI-SCHISTOSOMA SPECIES KIT (K842660) | Amico Lab, Inc. | 1984-10-30 |
| AMIZYME-SCHISTOSOMA SPP. TEST KIT (K842527) | Amico Lab, Inc. | 1984-09-05 |
Track GNH automatically
Every clearance here is in the API, with alerts when new ones post.