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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
510(K) Number: K031333
 
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FD 10/10 X-Ray System, Angiograph, bi-plane digital Allura FD, 10' detector 2 01/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Allura X-per FD 10/10 x-ray, and fluoroscopy 2 11/14/2006 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Allura Xper FD10/10 x-ray system 2 02/28/2006 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Allura X-ray System. The Allura X-ray System is an angiographic X-ray system. 2 04/25/2012 FEI # 1218950
Philips Healthcare Inc.
Allura Xper Systems Models: Allura Xper FD10 (F/C)-Biplane Fixed Allura Xper FD10/10 (incl. OR ta... 2 08/10/2011 FEI # 1218950
Philips Healthcare Inc.
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applica... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
NTEGRIS Allura 9 0 FDXD, System Code 722498 Vascular, cardiovascular and neurovascular imaging ... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
INTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular and neurovascular imagi... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
INTEGRIS CV, System Code 722030 Vascular, cardiovascular and neurovascular imaging applications,... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular, cardiovascular and neurovascular imag... 2 09/21/2018 FEI # 1218950
Philips Electronics North America Corporation
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