Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K012171 |
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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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The eCareManager system. Software intended for use in data collection, storage and clinical informa... | 2 | 12/10/2015 | Visicu, Inc. |
Philips eCareManager System, Model 865325, software versions 3.7, 3.7.1 and 3.8. Product Usage:... | 2 | 04/27/2012 | Visicu, Inc. |
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