Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K092449 |
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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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DPM 6 Monitor in use with a Multi Parameter Module (MPM). Patient monitor used for monitoring, disp... | 2 | 05/13/2014 | Mindray DS USA, Inc. dba Mindray North America |
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/... | 2 | 12/19/2014 | Mindray DS USA, Inc. dba Mindray North America |
DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA, Inc. 800 MacArthur Blvd. Ma... | 2 | 12/11/2012 | Mindray DS USA, Inc. d.b.a. Mindray North America |
Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Int... | 2 | 09/04/2015 | Mindray DS USA, Inc. dba Mindray North America |
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