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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K973482
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INTEGRIS H5000; Model Number: 72246 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS BV5000: Model Number: 72249 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS V5000: Model Number: 72248 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS BH5000; Model Number: 72247 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 01/30/2016 Philips Electronics North America Corporation
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