Continental Medical Labs,Inc
3 FDA 510(k) clearances · Recalling firm
◉ Watch Continental Medical Labs,Inc
| Record | Firm | Date |
|---|---|---|
| Blood Center Kit w/Chloraprep One-Step, Sterile/Disposable/Single Patient Use, Reorder No. recall (Z-0894-2011) | Continental Medical Labs,Inc | 2011-01-11 |
| Xenon Diagnostic Circuit Kits labeled as "Xenon Diagnostic Circuit", "Xenon Circuit", and recall (Z-1754-2010) | Continental Medical Labs,Inc | 2010-06-03 |
| Fibrin Analysis Catheter Testing System includes the component BD Vacutainer Luer-Lok Acce recall (Z-0357-2007) | Continental Medical Labs,Inc | 2007-01-18 |
Track Continental Medical Labs,Inc automatically
Every clearance here is in the API, with alerts when new ones post.