Medical Device Recalls
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1 result found
510(K) Number: K864385 |
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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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| Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 ... | 2 | 06/06/2007 | Vision Systems Group, A Div of Viking Systems |
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