GGQ
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Test, Prothrombin Consumption
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.7720
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| QUANTICHECK CONTROL PLASMA (K803081) | Abbott Laboratories | 1981-03-17 |
| A-GENT QUANTICHROM THROMBIGEN-E (K800656) | Abbott Laboratories | 1980-05-30 |
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Every clearance here is in the API, with alerts when new ones post.