Medical Device Recalls
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1 result found
510(K) Number: K131225 |
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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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Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventiona... | 2 | 10/01/2013 | Cordis Corporation |
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