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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K142999
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indica... 2 06/25/2015 FEI # 3010813691
ArthroCare Medical Corporation
PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices are ind... 2 06/25/2015 FEI # 3010813691
ArthroCare Medical Corporation
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