Medical Device Recalls
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1 result found
510(K) Number: K190969 |
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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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OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Ol... | 2 | 02/11/2022 | Olympus Corporation of the Americas |
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