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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K090672
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Agfa Healthcare NX 3.0.8950 Imaging Processing Software 2 07/14/2017 AGFA Healthcare Corp.
NX 2008 Central Monitoring System (CMS). Product code: E2FB6 Agfa's Computed Radiography System... 2 09/02/2009 AGFA Corp.
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