Medical Device Recalls
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1 result found
510(K) Number: K192898 |
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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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ASC PneumoLiner device, Part No. WA90500US (US market only) The Pneumoliner device is intended fo... | 2 | 10/26/2021 | Olympus Corporation of the Americas |
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