Medical Device Recalls
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1 result found
510(K) Number: K150272 |
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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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Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN0... | 2 | 12/01/2020 | Covidien Llc |
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