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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