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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K032046
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Philips Omni Diagnost Eleva 2 09/25/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Philips OmniDiagnost Eleva X-Ray System is a diagnostic imaging device intended for radiographic, fl... 2 09/16/2008 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
OminDiagnost Eleva 2 09/24/2009 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Philips OmniDiagnost Eleva with Digital Image (DI) Rel.2 system. The Philips OmniDiagnost Eleva i... 2 01/18/2011 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
Philips OmniDiagnost Eleva, a diagnostic-imaging device intended for radiographic, fluoroscopic, ang... 2 03/16/2011 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028 2 06/27/2018 FEI # 3002807880
Philips Medical Systems Nederlands
URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost ... 2 03/23/2019 FEI # 1218950
Philips North America, LLC
OmniDiagnost Eleva System codes 708028 708027 2 03/13/2020 FEI # 1218950
Philips North America, LLC
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