Medical Device Recalls
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1 result found
510(K) Number: K031903 |
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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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| Guidant RAPIDO Cut-Away Guiding Catheter, 6F. Part Numbers: 66676-201 and 667552-100. For ... | 2 | 07/12/2011 | Abbott Vascular |
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