Medical Device Recalls
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1 result found
510(K) Number: K120780 |
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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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Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage:... | 2 | 05/14/2013 | Edwards Lifesciences, LLC |
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