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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: K030697
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DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Electrode Kits (containing DGPHP RFA... 2 08/29/2012 FEI # 2936999
Nellcor Puritan Bennett Inc. (dba Covidien LP)
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