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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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AlluraXperFD20/15 System Code: (1) 722058 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
AlluraXperFD20/10 System Code: (1) 722029 2 02/04/2025 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.
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 2 02/04/2025 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.
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10C System Code: (1) 722001 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura CV20 System Code: 722031 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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