Medical Device Recalls
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1 result found
510(K) Number: K132914 |
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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 ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr. Model 8104, 8105, 8106, 8107, 810... | 2 | 01/05/2016 | Boston Scientific Corporation |
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