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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
510(K) Number: K200917
 
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Azurion 2 09/07/2023 Philips Medical Systems Nederland B.V.
Azurion 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and mi... 2 02/22/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and min... 2 02/22/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.0... 2 01/30/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.0... 2 01/30/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20. X-ray Image guided Therapy System. 2 08/02/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 with a Certeray generator-To perform image guidance in diagnostic, interventional, and min... 2 02/22/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion systems with software release R2.0.x 2 03/23/2022 Philips Healthcare
Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura Xper FD10C 722003 Allur... 2 12/15/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva syste... 2 09/14/2023 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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