Medical Device Recalls
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1 result found
510(K) Number: K141756 |
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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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Omega Systems These devices are intended to be used in the environment where patient care is prov... | 2 | 03/05/2019 | Draegar Medical Systems, Inc. |
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