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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 23 Results
510(K) Number: K080927
 
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BrightView X, Gamma Camera, Product Code 882478 2 01/05/2024 FEI # 3006648320
Philips North America
BrightView XCT, Gamma Camera, Product Code 882482 2 01/05/2024 FEI # 3006648320
Philips North America
BrightView X , Model Number 882478 2 07/22/2019 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView XCT , Model Number 882482 2 07/22/2019 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView SPECT, Model Number 882480 2 07/22/2019 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView X upgraded to XCT 882454 2 02/10/2017 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView XCT 2 02/10/2017 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView XCT Upgrade Model 882454 2 09/03/2016 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView XCT Model 882482, gamma camera for Single Photon Emission Computed Tomography (SPECT) 2 09/03/2016 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
BrightView XCT & BrightView XCT Upgrade, gamma cameras; For Single Proton Emission Computed Tomograp... 2 02/26/2016 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
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