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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K062641
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FDA Recall
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Avazzia Tennant Biomodulator®; Model: BEST AV-1; P/N #TB04303-103; manufactured by Avazzia, Inc., Da... 3 09/01/2007 Avazzia, Inc
Avazzia Med-Sport Massager; Model: BEST AV-1; P/N #MS04182-103; manufactured by Avazzia, Inc., Dalla... 3 09/01/2007 Avazzia, Inc
Avazzia BEST-RSI; Model: BEST AV-1; P/N #RS04303-103; manufactured by Avazzia, Inc., Dallas, TX 752... 3 09/01/2007 Avazzia, Inc
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