Medical Device Recalls
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1 result found
510(K) Number: K100705 |
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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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Z-800 Volumetric Infusion System. For intravenous infusion of parenteral fluids, blood and blood ... | 2 | 03/29/2013 | Zyno Medical LLC |
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