K.M.S., Inc. is one of 329 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
K.M.S., Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
K.M.S., Inc. has 1 FDA 510(k) cleared medical devices. Based in Cheonan-Si, KR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by K.M.S., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K.M.S., Inc.
1 devices