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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