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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K150708
 
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2008T Hemodialysis System without CDX 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T HD SYS. W/O CDX BLUESTAR 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T HD SYS. CDX W/BIBAG BLUESTAR 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T HD SYS. CDX BLUESTAR 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T Hemodialysis SYS, with CDX 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T HD SYS. W/O CDX W/BIBAG BLUESTAR 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T Hemodialysis System w/Bibag 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T GEN 2 Bibag without CDX 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
Fresenius 2008K@home Series : Hemodialysis System 2 01/13/2017 Fresenius Medical Care Renal Therapies Group, LLC
Fresenius 2008K2 Series : Hemodialysis System 2 01/13/2017 Fresenius Medical Care Renal Therapies Group, LLC
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