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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K003064
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cobas c 701 and 702 Analyzer/Module-RF interference claims for the sTfR assay Catalog Number: 05950... 2 10/09/2019 FEI # 1823260
Roche Diagnostics Operations, Inc.
cobas c 311; cobas c 501, 502,and COBAS INTEGRA 400 plus Analyzer/Module-RF interference claims for ... 2 10/09/2019 FEI # 1823260
Roche Diagnostics Operations, Inc.
Roche Diagnostics STFR Tina-quant Soluble Transferrin Receptor, COBAS INTEGRA, cobas c systems, Roch... 2 10/09/2008 FEI # 1823260
Roche Diagnostics Corp.
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