CJQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Radial Immunodiffusion, Albumin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1035
- Medical specialty
- Clinical Chemistry
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| HUMAN IGG-ALBUMIN TEST KIT (K811178) | Meloy Laboratories, Inc. | 1981-05-15 |
Track CJQ automatically
Every clearance here is in the API, with alerts when new ones post.