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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K092449
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Product Description
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FDA Recall
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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
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
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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