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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: K022118
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IMMULITE®/IMMULITE® Turbo 1000 CK-MB LSKCP --- Catalog number: LSKCP1 (100 tests), LSKCP5 (500 tests... 2 03/21/2012 Siemens Healthcare Diagnostics
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