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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 CV20 System Code: 722031 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura CV20; Catalog numbers: 722031 1 02/20/2025 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.
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026, 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10 and FD20. X-ray Imaging System. 2 08/02/2023 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027. 1 02/20/2025 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 Xper FD10C; Catalog number: 722001 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025. 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013. 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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