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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: K014209
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Product Description
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ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICA... 1 12/04/2014 FEI # 3001451571
ConMed Corporation
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO PHILIPS MEDI... 1 12/04/2014 FEI # 3001451571
ConMed Corporation
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MED... 1 12/04/2014 FEI # 3001451571
ConMed Corporation
PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. The PadPro(R... 2 05/13/2013 FEI # 3001451571
ConMed Corporation
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