Medical Device Recalls
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1 result found
510(K) Number: K032050 |
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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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| PeriVac® brand Pericardial Fluid Aspiration Procedure Kit (Pericardiocentensis Kit), with Pigtail Dr... | 2 | 10/30/2003 | Boston Scientific |
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