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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 31 Results
510(K) Number: K162859
 
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Allura Xper FD10 and FD20. X-ray Imaging System. 2 08/02/2023 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper series 2 09/07/2023 FEI # 3000976525
Philips Medical Systems Nederland B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c... 2 02/16/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line ... 2 02/16/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c... 2 02/16/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Versio... 2 05/24/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, Software Versio... 2 05/24/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Softwar... 2 05/24/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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