Kowa Co. , Ltd.
FDA 510(k) & PMA Approved Devices — 15 products
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Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112330 | KOWA VX-20 | HKI | 2012-02-16 | View |
| 510(k) | K101628 | KOWA NONMYD WX | HKI | 2011-01-26 | View |
| 510(k) | K091098 | KOWAGENESIS-DF | HKI | 2009-08-07 | View |
| 510(k) | K091039 | KOWA, FM-600, MODEL LSS50 | MYC | 2009-08-07 | View |
| 510(k) | K091683 | KOWA VX-10 A | HKI | 2009-07-02 | View |
| 510(k) | K083387 | MODIFICATION TO KOWA NONMYD ALPHA-DIII | HKI | 2009-01-16 | View |
| 510(k) | K082767 | KOWA NONMYD ALPHA-DIII | HKI | 2008-10-21 | View |
| 510(k) | K080681 | KOWA GENESIS-D | HKI | 2008-04-04 | View |
| 510(k) | K063640 | KOWA SL-15 | HJO | 2006-12-18 | View |
| 510(k) | K062021 | KOWA VX-10I | HKI | 2006-11-01 | View |
| 510(k) | K062356 | KOWA NONMYD ALPHA-D | HKI | 2006-09-27 | View |
| 510(k) | K053444 | KOWA KT-800 | HKX | 2006-06-09 | View |
| 510(k) | K053026 | KOWA NONMYD 7, KOWA NONMYD A-D | HKI | 2005-11-10 | View |
| 510(k) | K050271 | KOWA GENESIS-D HAND-HELD RETINAL CAMERA | HKI | 2005-11-03 | View |
| 510(k) | K043213 | KOWA VX-10 | HKI | 2005-10-06 | View |
No matching devices.
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