Company ยท JP
Kowa Co. , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2022. Name variants (Inc, Corp, punctuation) are merged.
19510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 21, 2022 | K222372 | Kowa SL-19 Kowa Company , Ltd., JP | HJO |
| Sep 10, 2019 | K191945 | KOWA nonmyd 8 Kowa Company , Ltd., JP | HKI |
| Jun 4, 2019 | K190573 | KOWA DR-1a Kowa Company , Ltd., JP | HKI |
| Mar 11, 2014 | K133755 | KOWA SL-17 Kowa Co. , Ltd., JP | HJO |
| Feb 16, 2012 | K112330 | KOWA VX-20 Kowa Co. , Ltd., JP | HKI |
| Jan 26, 2011 | K101628 | KOWA NONMYD WX Kowa Co. , Ltd., JP | HKI |
| Aug 7, 2009 | K091098 | KOWAGENESIS-DF Kowa Co. , Ltd., JP | HKI |
| Aug 7, 2009 | K091039 | KOWA, FM-600, MODEL LSS50 Kowa Co. , Ltd., JP | MYC |
| Jul 2, 2009 | K091683 | KOWA VX-10 A Kowa Co. , Ltd., JP | HKI |
| Jan 16, 2009 | K083387 | MODIFICATION TO KOWA NONMYD ALPHA-DIII Kowa Co. , Ltd., JP | HKI |
| Oct 21, 2008 | K082767 | KOWA NONMYD ALPHA-DIII Kowa Co. , Ltd., JP | HKI |
| Apr 4, 2008 | K080681 | KOWA GENESIS-D Kowa Co. , Ltd., JP | HKI |
| Dec 18, 2006 | K063640 | KOWA SL-15 Kowa Co. , Ltd., JP | HJO |
| Nov 1, 2006 | K062021 | KOWA VX-10I Kowa Co. , Ltd. | HKI |
| Sep 27, 2006 | K062356 | KOWA NONMYD ALPHA-D Kowa Co. , Ltd., JP | HKI |
| Jun 9, 2006 | K053444 | KOWA KT-800 Kowa Co. , Ltd., JP | HKX |
| Nov 10, 2005 | K053026 | KOWA NONMYD 7, KOWA NONMYD A-D Kowa Co. , Ltd., JP | HKI |
| Nov 3, 2005 | K050271 | KOWA GENESIS-D HAND-HELD RETINAL CAMERA Kowa Co. , Ltd., JP | HKI |
| Oct 6, 2005 | K043213 | KOWA VX-10 Kowa Co. , Ltd. | HKI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||