Zoll Lifecor Corporation
4 FDA 510(k) clearances · Recalling firm
◉ Watch Zoll Lifecor Corporation
| Record | Firm | Date |
|---|---|---|
| Model 4000 Monitor component of the LifeVest Wearable Defibrillator recall (Z-0625-2011) | Zoll Lifecor Corporation | 2010-12-16 |
| Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit as recall (Z-0883-2009) | Zoll Lifecor Corporation | 2009-01-28 |
| Battery Pack portion of the LifeVest device. The LifeVest is a wearable cardioverter defib recall (Z-0061-2008) | Zoll Lifecor Corporation | 2007-10-18 |
| Electrode Belt, component of the LifeVest Wearable Defibrillator, Product number 10A0889-A recall (Z-0936-2007) | Zoll Lifecor Corporation | 2007-06-15 |
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Every clearance here is in the API, with alerts when new ones post.