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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Date Classified to: 12/21/2014 510(K) Number: K040049
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Product Description
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Recall
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Recalling Firm
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Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060... 2 Sep-20-2013 Steris Corporation
Steris Reliance EPS Endoscope Processing System , manufactured by Corporation STERIS Canada, Quebec,... 3 Dec-28-2010 Steris Corporation
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