Medical Device Recalls
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1 result found
510(K) Number: K150882 |
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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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Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal... | 2 | 04/27/2016 | Mindray DS USA, Inc. dba Mindray North America |
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