Medical Device Recalls
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1 result found
510(K) Number: K915265 |
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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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CDI® H/S Cuvette The intended use for the CDI® H IS Cuvette is as follows: The CDI® H/S Cuvettes ... | 3 | 10/03/2016 | Terumo Cardiovascular Systems Corporation |
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