Micrel Medical Devices S.A. - FDA 510(k) Cleared Devices

Micrel Medical Devices S.A. has 1 FDA 510(k) cleared medical devices. Based in Pallini, GR.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Micrel Medical Devices S.A. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.