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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K113276
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Recall
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FDA Recall
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PC Application Software c4D as part of the device Catalyst: SP-002 Software PA-003 version 6.1.1 and... 2 07/14/2021 FEI # 3006621300
C-RAD POSITIONING AB
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