Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K895715 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HANAULUX 2004 IXL cupola, P/N: 56076868 Intended to provide visible illumination for the surgical... | 2 | 11/12/2009 | MAQUET Inc. |
HANAULUX 2004-2005 TV Spring Arm, P/N: 569002998. Intended to provide visible illumination for th... | 2 | 11/12/2009 | MAQUET Inc. |
HANAULUX 2005 IXL cupola, P/N: 56076869. Intended to provide visible illumination for the surgica... | 2 | 11/12/2009 | MAQUET Inc. |
HANAULUX 2005 I cupola, P/N: 56076865. Intended to provide visible illumination for the surgical ... | 2 | 11/12/2009 | MAQUET Inc. |
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