Medical Device Recalls
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1 result found
510(K) Number: K173519 |
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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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| 3M Attest Super Rapid Readout Steam Challenge Pack, REF 1496V; designed to qualify and monitor dynam... | 2 | 09/26/2023 |
FEI # 2110898 3M Company - Health Care Business |
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