Medical Device Recalls
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1 result found
510(K) Number: K895770 |
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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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Exel Huber Infusion Set (Catalog Numbers 26940R, 26941R, 26944R, 26945R, 26946R, 26948R, 26949R, 269... | 1 | 01/22/2010 | Exelint International Co. |
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