Medical Device Recalls
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1 result found
510(K) Number: K102699 |
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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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| ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnos... | 2 | 05/12/2020 |
FEI # 3002809144 Abbott Gmbh & Co. KG |
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