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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K082515
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Asahi KASEI, REXEED(TM)- 13 LX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 15 SX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 18 SX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
Asahi KASEI, REXEED(TM)- 25 SX, HEMODIALYZER dialysis filter 2 09/20/2012 Asahi Kasei Medical Co., Ltd., Okatomi Plant
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