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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: K023304
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IMMULITE Calcitonin Control Module (IMMULITE, IMMULITE 1000, IMMULITE 2000, IMMULITE 2000 XPi) Fo... 3 11/13/2014 Siemens Healthcare Diagnostics, Inc.
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