ZOLL Medical Corporation, World Wide Headquarters
4 FDA 510(k) clearances · Recalling firm
◉ Watch ZOLL Medical Corporation, World Wide Headquarters
| Record | Firm | Date |
|---|---|---|
| ZOLL E Series Defibrillator/Pacemaker/Monitors, BLS Model, with software versions 4.XX, 6. recall (Z-1547-2010) | ZOLL Medical Corporation, World Wide Headquarters | 2010-05-07 |
| ZOLL R Series Defibrillator/Pacemaker/Monitor Used by qualified medical personnel for the recall (Z-2315-2009) | ZOLL Medical Corporation, World Wide Headquarters | 2009-09-29 |
| Zoll AED Plus Defibrillator recall (Z-1206-2009) | ZOLL Medical Corporation, World Wide Headquarters | 2009-04-01 |
| Zoll E Series Defibrillator with 12 Lead ECG, Automated external defibrillator, Software V recall (Z-1167-2008) | ZOLL Medical Corporation, World Wide Headquarters | 2008-06-28 |
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Every clearance here is in the API, with alerts when new ones post.