Medical Device Recalls
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1 result found
510(K) Number: K101777 |
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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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Volcano Pioneer Plus Re-Entry Catheter; Product Code PPLUS20, Catheter for Crossing Total Occlusion... | 2 | 09/02/2015 | Volcano Corporation |
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