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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 42 Results
510(K) Number: K141979
 
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Allura Xper FD10, FD10 C, and FD10 F; Model Numbers: 722026 722010 722003 722002 722001 Intended... 2 01/30/2016 Philips Electronics North America Corporation
Cardiovascular Allura Centron; Model Number: 722400 The Allura CV2O is intended for physicians (... 2 01/30/2016 Philips Electronics North America Corporation
Allura CV20; Model Number: 722031 The Allura CV2O is intended for physicians (e.g. cardiologists ... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD20/20 OR Table; Model Number: 722039 Dedicated vascular and neurovascular imaging... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD10/10; Model Numbers: 722027 722011 722005 Intended for Cardiovascular and vascular... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD10 OR Table; Model Numbers: 722033 722022 Intended for Cardiovascular and vascular ... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD20/10; Model Numbers: 722029 Dedicated vascular and neurovascular imaging applicati... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD20/15; Model Numbers: 722058 Dedicated vascular and neurovascular imaging applicati... 2 01/30/2016 Philips Electronics North America Corporation
Allura Xper FD20; Model Numbers: 722028 722012 722006 Dedicated vascular and neurovascular imagin... 2 01/30/2016 Philips Electronics North America Corporation
UNIQ FD; Model Numbers: 722028 The Philips UNIQ is intended for use on human patients to perform:... 2 01/30/2016 Philips Electronics North America Corporation
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