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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 54 Results
510(K) Number: K033737
 
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Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY); 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/10; Catalog numbers: 722029 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/15; Catalog numbers: 722058 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20/20; Catalog numbers: 722038 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura CV20; Catalog numbers: 722031 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(OUS ONLY). 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035. 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY). 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013. 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028. 1 02/20/2025 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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