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FDA 510(k) Applications Submitted by AKIHIRO FUJITA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091683
06/10/2009
KOWA VX-10 A
KOWA CO. LTD.
K082767
09/22/2008
KOWA NONMYD ALPHA-DIII
KOWA CO. LTD.
K083387
11/17/2008
MODIFICATION TO KOWA NONMYD ALPHA-DIII
KOWA CO. LTD.
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