Medical Device Recalls
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1 result found
510(K) Number: K070005 |
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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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HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluatio... | 2 | 07/22/2013 | Instrumentation Laboratory Co. |
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