Cardima Inc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Cardima Surgical Ablation Probe (SAP) Electrosurgical cutting and coagulation device, Mode recall (Z-2580-2010) | Cardima Inc | 2010-09-27 |
| Cardima Surgical Ablation Probe (SAP) Electrosurgical cutting and coagulation device, Mode recall (Z-2581-2010) | Cardima Inc | 2010-09-27 |
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Every clearance here is in the API, with alerts when new ones post.