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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 31 Results
510(K) Number: K162859
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Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 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.
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 2 02/04/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Versio... 2 05/24/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, Software Versio... 2 05/24/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Softwar... 2 05/24/2024 FEI # 3002807880
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 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line ... 2 02/16/2024 FEI # 3002807880
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 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper series 2 09/07/2023 FEI # 3000976525
Philips Medical Systems Nederland B.V.
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