St. Jude Medical, Atrial Fibrillation Division, Inc.
2 FDA 510(k) clearances · Recalling firm
◉ Watch St. Jude Medical, Atrial Fibrillation Division, Inc.
| Record | Firm | Date |
|---|---|---|
| TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an recall (Z-0814-2024) | St. Jude Medical, Atrial Fibrillation Division, Inc. | 2024-01-25 |
| St. Jude Medical Epicor UltraWand LP Handheld Ablation Device, model UW-LP-2, Sterilized w recall (Z-1780-2010) | St. Jude Medical Atrial Fibrillation Division Inc | 2010-06-07 |
Track St. Jude Medical, Atrial Fibrillation Division, Inc. automatically
Every clearance here is in the API, with alerts when new ones post.