Levitronix, Llc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Levitronix CentriMag Primary System, Article Number: 201-30100; extracorporeal blood circu recall (Z-1901-2008) | Levitronix, Llc | 2008-07-23 |
| Levitronix CentriMag Back-Up Console Article Number: 201-30200; extracorporeal blood circu recall (Z-1902-2008) | Levitronix, Llc | 2008-07-23 |
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Every clearance here is in the API, with alerts when new ones post.