Kowa Co. , Ltd.
Kowa Co. , Ltd. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2014.
Top product codes for Kowa Co. , Ltd.
Recent clearances by Kowa Co. , Ltd.
- K133755 — KOWA SL-17
- K112330 — KOWA VX-20
- K101628 — KOWA NONMYD WX
- K091039 — KOWA, FM-600, MODEL LSS50
- K091098 — KOWAGENESIS-DF
- K091683 — KOWA VX-10 A
- K083387 — MODIFICATION TO KOWA NONMYD ALPHA-DIII
- K082767 — KOWA NONMYD ALPHA-DIII
- K080681 — KOWA GENESIS-D
- K063640 — KOWA SL-15
- K062021 — KOWA VX-10I
- K062356 — KOWA NONMYD ALPHA-D
- K053444 — KOWA KT-800
- K053026 — KOWA NONMYD 7, KOWA NONMYD A-D
- K050271 — KOWA GENESIS-D HAND-HELD RETINAL CAMERA
- K043213 — KOWA VX-10
Data sourced from openFDA. This site is unofficial and independent of the FDA.