Medical Device Recalls
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1 result found
510(K) Number: K143474 |
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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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| Quest Spectrum 3 Fluorescent Imaging System Model/Catalog Number: ART-SYS-0029, ART-SYS-0030 Th... | 2 | 10/25/2024 | Olympus Corporation of the Americas |
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