Medical Device Recalls
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1 result found
510(K) Number: K162227 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Produ... | 2 | 03/19/2026 |
FEI # 2245451 Diagnostica Stago, Inc. |
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