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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: K023251
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Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 ... 2 08/15/2012 FEI # 3008355164
Maquet Inc.
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