Medical Device Recalls
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1 result found
510(K) Number: K000956 |
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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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Boston Scientific, Impulse Angiographic Catheter, Sterile EO. Catheters are single lumen catheters ... | 2 | 01/31/2008 | Boston Scientific |
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