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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
Recall Date to: 09/01/2014 510(K) Number: K132304
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Product Description
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FDA Recall
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Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... 2 03/20/2014 Philips Medical Systems North America Inc.
Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... 2 03/20/2014 Philips Medical Systems North America Inc.
EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imagin... 2 11/20/2013 Philips Medical Systems North America Inc.
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