Medical Device Recalls
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1 result found
510(K) Number: K874896 |
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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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Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes an... | 2 | 07/23/2014 | Terumo Cardiovascular Systems Corporation |
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