Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K062451 |
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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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NeuViz 16 Multi-Sliced CT Scanner System, part number 989605858501. NeuViz Dual series CT Scanner S... | 2 | 12/04/2012 | Philips And Neusoft Medical Systems Co., Ltd. |
The device is the NeuViz Dual series Computed Tomography (CT) Scanner System. The device is identif... | 2 | 01/04/2011 | Philips And Neusoft Medical Systems Co., Ltd. |
NeuViz Dual series Computed Tomography (CT) Scanner System, X-Ray System. Part Number: 989605651321... | 2 | 08/19/2010 | Neuisys, LLC |
NeuViz Dual Multi-Slice Computed Tomography (CT) Scanner System (software). Whole body x-ray comp... | 2 | 01/26/2009 | Philips Medical Systems North America Co. Phillips |
NeuViz Dual series computed Tomography Scanner System, X-Ray System | 2 | 09/17/2008 | Philips And Neusoft Medical Systems Co., Ltd. |
NeuViz Dual series computed Tomography Scanner System, X-Ray System The CT scanner is a whole body ... | 2 | 09/17/2008 | Philips And Neusoft Medical Systems Co., Ltd. |
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