8
Total
8
Cleared
0
Denied

Actherm, Inc. has 8 FDA 510(k) cleared medical devices. Based in Jubei, Hsinchu, TW.

Historical record: 8 cleared submissions from 2001 to 2010. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Actherm, Inc. Filter by specialty or product code using the sidebar.

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

FDA 510(k) Regulatory Record - Actherm, Inc.

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