Medical Device Recalls
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1 result found
510(K) Number: K032137 |
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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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This medical device is packaged in an inner Tyvek pouch and then in an outer carton. The outer cart... | 1 | 07/20/2004 | Cordis Corporation |
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