Medical Device Recalls
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1 result found
510(K) Number: K983475 |
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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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Hemochron Whole Blood Coagulation Systems Activated Clotting Time (ACT); Package label states -Inter... | 2 | 02/11/2011 | International Technidyne Corp. |
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