Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K033441 |
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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, RunWay Guide Catheter, UPN H749389696640, Catalog Number 38969-664. | 2 | 03/10/2014 | Boston Scientific Corporation |
RunWay 6F Cardiovascular Guide Catheter. | 2 | 01/28/2005 | Boston Scientific Scimed |
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