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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: K944211
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IMMULITE/IMMULITE 1000 Progesterone (LKPG 1,5) For in vitro diagnostic use with the IMMULITE and ... 2 12/23/2008 FEI # 3005250747
Siemens Medical Solutions Diagnostics
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