Medical Device Recalls
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1 result found
510(K) Number: K070266 |
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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 560P High Definition Camera Control Unit Catalog Number: 72201919 The 560P camera s... | 2 | 05/01/2012 | Smith & Nephew, Inc. Endoscopy Division |
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