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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 34 Results
510(K) Number: K102005
 
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Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K1... 2 09/25/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD OR Table, Ceiling version only; 722035; imaging applications. 2 02/05/2016 Philips Electronics North America Corporation
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K10200... 2 09/25/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: K102005, ... 2 09/25/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005; Associated 510(k) numbers: K10... 2 09/25/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722005; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722011; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10/10; Model Number: 722027; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10; Model Number: 722003; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD10; Model Number: 722010; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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