Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K031760 |
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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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Panaroma Central Station Product Usage: This device can view real time, store, print, graph, a... | 2 | 03/07/2014 | Mindray DS USA, Inc. dba Mindray North America |
Panorama Patient Monitoring Network with ambulatory telepacks, and software version 8.5.5, 8.5.6, 8.... | 2 | 05/27/2009 | Mindray DS USA, Inc., dba Datascope Patient Monitoring |
Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor. | 2 | 01/24/2006 | Datascope Corp |
Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor. | 2 | 09/21/2005 | Datascope Corp |
Panorama Patient Monitoring Network. Cardiac Arrhythmia Monitor. | 2 | 08/06/2005 | Datascope Corp |
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