Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K830755 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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IV Sets and Accessories, various configurations. An Intravenous Administration Tubing set is a de... | 1 | 03/30/2010 | Arrow International Inc |
150ML Burette IV Set with SmartSite(TM) Y-Injection Site, 2-Gang Standard Bore Stopcocks and T-Conne... | 1 | 03/30/2010 | Arrow International Inc |
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