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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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Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release ... 2 04/05/2022 Philips Healthcare
Azurion systems with software release R2.0.x 2 03/23/2022 Philips Healthcare
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) 2 11/24/2021 Philips Healthcare
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 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 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and mi... 2 02/22/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC compo... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC compo... 2 02/16/2024 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.
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