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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K251061
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NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdens... 2 02/03/2026 FEI # 2240869
Siemens Medical Solutions USA, Inc
NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperde... 2 02/03/2026 FEI # 2240869
Siemens Medical Solutions USA, Inc
NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensitie... 2 02/03/2026 FEI # 2240869
Siemens Medical Solutions USA, Inc
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