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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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Philips Medical System Allura Xper X-Ray Angiographic 2 03/02/2015 Philips Medical Systems, Inc.
Product Name: Allura Xper FD10C; Model number: 722001; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20; Model Number: 722038; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; Model Number: 722029; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722028; 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: 722026; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 OR Table; Model Number: 722023; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane; Model Number: 722013; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Model Number: 722012; 2 01/13/2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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