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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K053502
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Recall
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FDA Recall
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Newport e360 Ventilator, Model Number: e360 The e360 Ventilator System is intended to provide con... 2 06/08/2011 Newport Medical Instruments Inc
Newport e360 Ventilator The e360 Ventilator System is intended to provide continuous (endotrachea... 2 05/19/2010 Newport Medical Instruments Inc
Newport e360 Ventilator, Rx only. The e360 Ventilator System is intended to provide continuous ... 2 09/04/2009 Newport Medical Instruments Inc
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