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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: K183432
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Cobas u 601 urinalysis test system, Catalog number 06334601001 The cobas U 601 urinalysis test syst... 2 11/18/2021 FEI # 1823260
Roche Diagnostics Operations, Inc.
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