Skytron, Div. the Kmw Group, Inc. - FDA 510(k) Cleared Devices

Skytron, Div. the Kmw Group, Inc. has 19 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.

Historical record: 19 cleared submissions from 1981 to 2007.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.