Medical Device Recalls
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1 result found
510(K) Number: K151080 |
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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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Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The Problem only affects CSM-1901... | 2 | 03/20/2017 | Nihon Kohden America Inc |
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