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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: K875353
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Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Repl... 2 06/26/2015 FEI # 1000116158
Medtronic Perfusion Systems
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