FDA 510(k) Applications Submitted by NIKKISO CO. LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K061519 06/01/2006 MODIFICATION TO DBB-05 HEMODIALYSIS DELIVERY SYSTEM NIKKISO CO. LTD.
K091978 07/01/2009 DBB-06 HEMODIALYSIS DELIVERY SYSTEM NIKKISO CO. LTD.
K082719 09/17/2008 NIKKLINE BLOOD TUBING LINES WITH TRANSDUCER PROTECTORS, MODELS AV06A-P, AVO6B-P, AV06C-P NIKKISO CO. LTD.
K953996 08/24/1995 NIKKISO CO, LTD., FLX10GW, 12GW, 15GW, 18GW & 21GW HEMODIALYZERS NIKKISO CO. LTD.


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