GKQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Test, Thromboplastin Generation
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.7900
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| FIBROSYSTEM (K823520) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1982-12-28 |
Track GKQ automatically
Every clearance here is in the API, with alerts when new ones post.