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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K133292
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AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 2 02/04/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC c... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line ... 2 02/16/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional... 2 05/01/2018 Philips Electronics North America Corporation
Allura Xper systems with Certeray X-ray Generator located in regions with high mains (480V) voltage.... 2 02/24/2018 Philips Electronics North America Corporation
Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD... 2 04/14/2017 Philips Electronics North America Corporation
Allura Xper FD20/15 R8.2 722058 is intended for: Cardiovascular and vascular X-ray imaging applicati... 2 01/20/2017 Philips Electronics North America Corporation
Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications... 2 01/20/2017 Philips Electronics North America Corporation
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