Actherm, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Actherm, Inc. - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Actherm, Inc.
8 devices
Cleared
Mar 12, 2010
ACTHERM INFRARED EAR THERMOMETER ACT 8000R SERIES AND ITS PROBE COVER MED...
General Hospital
92d
Cleared
Jul 16, 2009
ACTHERM DIGITAL CLINICAL THERMOMETER PROBE COVERS, MODEL(S) MEDACCU1010,...
General Hospital
239d
Cleared
Apr 16, 2009
ACTHERM INFRARED EAR THERMOMETER, ACT 8000 SERIES
General Hospital
101d
Cleared
Feb 08, 2007
CLASSIC/HYPOTHERMIA, FLEXIBLE, 10-SECOND, LEFT-RIGHT HANDED, BASAL,...
General Hospital
36d
Cleared
Jul 07, 2003
DIGITAL CLINICAL THERMOMETER, MODELS ACT2130, ACT 2230, ACT 2330, ACT 3136,...
General Hospital
17d
Cleared
May 30, 2002
DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038
General Hospital
14d
Cleared
May 30, 2002
DIGITAL CLINICAL THERMOMETER, MODEL ACT 3020
General Hospital
14d
Cleared
Feb 06, 2001
ACTHERM DIGITAL CLINICAL THERMOMETER, MODELS ACT2000, ACT2010, ACT2000+,...
General Hospital
12d