Medical Device Recalls
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1 result found
510(K) Number: K053234 |
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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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Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities. | 2 | 01/27/2013 | Mindray DS USA, Inc. d.b.a. Mindray North America |
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