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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K123299
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Percutaneous Trial Lead Kit Model 3086 (8 ch percutaneous lead). Used as part of the St. Jude Med... 2 09/29/2014 FEI # 1627487
St. Jude Medical, Inc.
Percutaneous Trial Lead Kit Model 3046 (4 ch percutaneous lead). Used as part of the St. Jude Med... 2 09/29/2014 FEI # 1627487
St. Jude Medical, Inc.
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