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FDA 510(k) Applications Submitted by Toshihiko Motomine
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160004
01/04/2016
Crosstella OTW
KANEKA CORPORATION
K160013
01/04/2016
Crosperio OTW
KANEKA CORPORATION
K170941
03/30/2017
RX NC Takeru PTCA Balloon Dilatation Catheter
Kaneka Corporation
K150865
04/01/2015
Metacross RX PTA Balloon Dilitation Catheter
Kaneka Corporation
K152080
07/27/2015
Metacross OTW PTA Balloon Dilatation Catheter
Kaneka Corporation
K172264
07/27/2017
OTW Takeru PTCA Balloon Dilatation Catheter
Kaneka Corporation
K152873
09/30/2015
Crosstella RX Balloon Dilatation Catheter
KANEKA CORPORATION
K152887
09/30/2015
Crosperio RX PTA Balloon Dilatation Catheter
Kaneka Corporation
K163372
12/01/2016
RX Takeru Balloon Dilatation Catheter
KANEKA CORPORATION
K163479
12/12/2016
R2P Metacross RX
KANEKA CORPORATION
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