Home / Companies / Kowa Co. , Ltd.

Kowa Co. , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133755KOWA SL-17March 11, 2014
K112330KOWA VX-20February 16, 2012
K101628KOWA NONMYD WXJanuary 26, 2011
K091098KOWAGENESIS-DFAugust 7, 2009
K091039KOWA, FM-600, MODEL LSS50August 7, 2009
K091683KOWA VX-10 AJuly 2, 2009
K083387MODIFICATION TO KOWA NONMYD ALPHA-DIIIJanuary 16, 2009
K082767KOWA NONMYD ALPHA-DIIIOctober 21, 2008
K080681KOWA GENESIS-DApril 4, 2008
K063640KOWA SL-15December 18, 2006
K062021KOWA VX-10INovember 1, 2006
K062356KOWA NONMYD ALPHA-DSeptember 27, 2006
K053444KOWA KT-800June 9, 2006
K053026KOWA NONMYD 7, KOWA NONMYD A-DNovember 10, 2005
K050271KOWA GENESIS-D HAND-HELD RETINAL CAMERANovember 3, 2005
K043213KOWA VX-10October 6, 2005