NBK
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- System, Test, (Ihc), Tumor Marker, Monitoring, Bladder Cancer
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.1860
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| IMMUNOCYT (K994356) | Diagnocure, Inc. | 2000-02-23 |
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Every clearance here is in the API, with alerts when new ones post.