Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951485 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AVOXimeter 1000, AVOXimeter 4000 1000- portable bedside whole blood oximeter that directly measures... | 2 | 05/19/2011 |
FEI # 1000526865 International Technidyne Corp. |
| International Technidyne Corp. (ITC) AVOXimeter 4000 Co-oximeter, Catalog Numbers: AVOX4000-110 an... | 2 | 08/06/2008 |
FEI # 1000526865 International Technidyne Corp. |
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