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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K162859
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Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035. 1 02/20/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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