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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: K902002
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Medtronic, Sutureless, unipolar, myocardial, screw-in pacing lead, 5071-15, 5071-25, 5071-35 & 5071-... 2 03/23/2010 FEI # 2182208
Medtronic Inc. Cardiac Rhythm Disease Managment
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