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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 31 Results
510(K) Number: K162859
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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.
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper series 2 09/07/2023 FEI # 3000976525
Philips Medical Systems Nederland B.V.
Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028. 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20; Catalog numbers: 722038 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20 System Code: (1) 722038 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15; Catalog numbers: 722058 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; Catalog numbers: 722029 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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