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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 17 Results
510(K) Number: K971365
 
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Poly G Integris H5000, System code 72246 2 03/13/2020 Philips North America, LLC
INTEGRIS V3000; Model Number: 72243, 72244, 72245 The Philips INTEGRIS 3000 I 5000 system is inte... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS BH3000; Model Number: 72242 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS BN/BV3000; Model Number: 72240 The Philips INTEGRIS 3000 I 5000 system is intended for i... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS HM3000; Model Number: 72239 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS H3000; Model Number: 72238 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 01/30/2016 Philips Electronics North America Corporation
INTEGRIS BV3000 MONO; Model Number: 72241 The Philips INTEGRIS 3000 I 5000 system is intended for... 2 01/30/2016 Philips Electronics North America Corporation
Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product Usage: The Allura Xper se... 2 12/01/2015 Philips Medical Systems, Inc.
Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Usage: The Allura Xper seri... 2 12/01/2015 Philips Medical Systems, Inc.
Philips Healthcare Xper vascular system Model : 722124 Product Usage: The Allura Xper series... 2 12/01/2015 Philips Medical Systems, Inc.
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