Medical Device Recalls
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1 result found
510(K) Number: K081217 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide solution, Part # 308051, ... | 2 | 10/29/2019 |
FEI # 1000125787 Hycor Biomedical LLC |
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