Medical Device Recalls
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1 result found
510(K) Number: K994084 |
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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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Smith & Nephew, 420XL Xenon Light Source, 180 Watt; for endoscopic use. Catalog/Part #72200510; manu... | 2 | 06/07/2007 | Smith & Nephew, Inc Endoscopy Division |
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