ITC-Nexus Dx
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Hemochron Jr. Whole Blood Microcoagulation System APTT Cuvette. For in vitro diagnostic co recall (Z-2088-2014) | ITC-Nexus Dx | 2014-07-21 |
| Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized microcoagulation test intende recall (Z-0937-2014) | ITC-Nexus Dx | 2014-02-06 |
Track ITC-Nexus Dx automatically
Every clearance here is in the API, with alerts when new ones post.