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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K964469
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CONMED PEDIATRIC R2 Multifunction Electrodes, REF/Catalog Number 3115-1750, Direct Connect to Philip... 1 12/04/2014 FEI # 3001451571
ConMed Corporation
CONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direct Connect to Philips He... 1 12/04/2014 FEI # 3001451571
ConMed Corporation
R2 Adult R2 Non-Radiolucent Multifunction Electrodes, Catalog/REF No. 3200-1715, NON-STERILE, MADE I... 2 01/25/2012 FEI # 3001451571
ConMed Corporation
R2 Adult Zoll Non-Radiolucent Multifunction Electrodes, Catalog/REF 3111-1721, NON-STERILE, ASSEMBLE... 2 01/12/2012 FEI # 3001451571
ConMed Corporation
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