Medical Device Recalls
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1 result found
510(K) Number: K102420 |
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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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Edwards Lifesciences EMBOL-X Glide Protection System; Model Numbers: EXGF24D, EXGF24LLD, EXGF24MMD, ... | 1 | 10/31/2013 | Edwards Lifesciences, LLC |
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