Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080192 |
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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 DS USA, Inc., DPM Central Monitoring System with ambulatory Telepack. Part numbers: 300BF-PA... | 2 | 02/11/2013 | Mindray DS USA, Inc. d.b.a. Mindray North America |
DPM Central Station Mindray DS USA, Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 The Central M... | 2 | 01/03/2013 | Mindray DS USA, Inc. d.b.a. Mindray North America |
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