JBN
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Fibrin Monomer Paracoagulation
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.7300
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| FS TEST KIT (K854015) | American Bioproducts Co. | 1986-03-06 |
| SULFATE, FIBRIQUIK PROTAMINE (K781814) | General Diagnostics | 1978-11-08 |
Track JBN automatically
Every clearance here is in the API, with alerts when new ones post.