Medical Device Recalls
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1 result found
510(K) Number: K190744 |
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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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Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video syst... | 2 | 01/10/2024 | Olympus Corporation of the Americas |
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