FDA 510(k) Applications Submitted by FUMIAKI KANAI

FDA 510(k) Number Submission Date Device Name Applicant
K080921 04/01/2008 SPIRO-MASTER PC-10 SPIROMETRY SYSTEM CHEST M.I., INC.
K111231 05/02/2011 PANOURA 18S THE YOSHIDA DENTAL MFG. CO., LTD.
K061519 06/01/2006 MODIFICATION TO DBB-05 HEMODIALYSIS DELIVERY SYSTEM NIKKISO CO. LTD.
K121901 06/29/2012 TI-MAX Z45 NAKANISHI, INC.
K091978 07/01/2009 DBB-06 HEMODIALYSIS DELIVERY SYSTEM NIKKISO CO. LTD.
K081953 07/09/2008 SUPERCATH 5 TOGO MEDIKIT CO., LTD.
K112290 08/09/2011 SUPERCATH Z3V TOGO MEDIKIT CO., LTD.
K052267 08/19/2005 SUPERCATH V TOGO MEDIKIT CO., LTD.
K082719 09/17/2008 NIKKLINE BLOOD TUBING LINES WITH TRANSDUCER PROTECTORS, MODELS AV06A-P, AVO6B-P, AV06C-P NIKKISO CO. LTD.
K072643 09/18/2007 CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US OLYMPUS CORPORATION
K093888 12/18/2009 COOPDECH ENDOBRONCHIAL BLOCKER TUBE DAIKEN MEDICAL CO, LTD.
K093546 11/17/2009 SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX TOGO MEDIKIT CO., LTD.
K120886 03/23/2012 LACRIFAST HIROYASU HIGUCHI


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