Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K022008 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cardima Surgical Ablation Probe (SAP) Electrosurgical cutting and coagulation device, Model Number 0... | 2 | 09/27/2010 | Cardima Inc |
| Cardima Surgical Ablation Probe (SAP) Electrosurgical cutting and coagulation device, Model Number 0... | 2 | 09/27/2010 | Cardima Inc |
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