Stierlen-Maquet AG - FDA 510(k) Cleared Devices

Stierlen-Maquet AG has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1984 to 1997.

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 Tuv Product Service, Inc. as regulatory consultant.