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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K140683
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Omnera 400A Digital Radiographic System 2 07/05/2022 FEI # 3002675731
Arcoma AB
Omnera 400T Digital Radiographic System 2 07/05/2022 FEI # 3002675731
Arcoma AB
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