Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K014241 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Alsius Cool Line Catheter, Model CL-2295AE | 2 | 02/15/2007 |
FEI # 3002922896 Alsius Corporation |
| Alsius Cool Line Catheter, Model CL-2295A | 2 | 02/15/2007 |
FEI # 3002922896 Alsius Corporation |
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