K.M.S., Inc. is one of 464 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
Recent clearances: KM Needles (Acupuncture Needle)
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.
510(k) submissions have been managed by International Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - K.M.S., Inc.
1 devices