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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 15 Results
510(K) Number: K033737
 
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Product Description
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Allura Xper FD2O Biplane, System Code 722013 Vascular, cardiovascular and neurovascular imaging ... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
Allura Xper FD2O Biplane, System Code 722008 Vascular, cardiovascular and neurovascular imaging ... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and neurovascular imaging applicat... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
Allura Xper FD2O, System Code 722012 Vascular, cardiovascular and neurovascular imaging applicat... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
Allura Xper FD20 722012 is intended for: Cardiovascular and vascular X-ray imaging applications, inc... 2 01/20/2017 FEI # 1218950
Philips Electronics North America Corporation
Velara Generator with an old Firmware version used with the Philips Integris BH5000 2 01/20/2017 FEI # 1218950
Philips Electronics North America Corporation
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications. 2 02/05/2016 FEI # 1218950
Philips Electronics North America Corporation
Philips Medical Systems Allura Xper FD20C Radiological Imaging with software version R8.2.O; System ... 2 11/07/2014 FEI # 1218950
Philips Medical Systems, Inc.
Philips Medical Systems Allura Xper FD20C with software version R8.2.O System Code: 722035. The ... 2 11/07/2014 FEI # 1218950
Philips Medical Systems, Inc.
Philips Allura XPER FD20 Angiographic X-ray system. This system with Velara Generator can be identi... 2 09/22/2010 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
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