Medical Device Recalls
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1 result found
510(K) Number: K904003 |
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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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RQCHRT HRT Control Level 1 & 2; Whole Blood controls for use with Hemochron Kaolin and Celite HRT T... | 2 | 07/28/2010 | International Technidyne Corp. |
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