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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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