Actherm, Inc.
Actherm, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2010.
Top product codes for Actherm, Inc.
Recent clearances by Actherm, Inc.
- K093795 — ACTHERM INFRARED EAR THERMOMETER ACT 8000R SERIES AND ITS PROBE COVER MED ACCU2010
- K083419 — ACTHERM DIGITAL CLINICAL THERMOMETER PROBE COVERS, MODEL(S) MEDACCU1010, MEDACCU1010-1, MEDACCU1020
- K090031 — ACTHERM INFRARED EAR THERMOMETER, ACT 8000 SERIES; PROBE COVER FOR ACTHERM INFRARED EAR THERMOMETER, MODEL MEDACCU2010
- K070028 — CLASSIC/HYPOTHERMIA, FLEXIBLE, 10-SECOND, LEFT-RIGHT HANDED, BASAL, LIGHTWEIGHT-PROBE DIGITAL CLINICAL THERMOMETER
- K031905 — DIGITAL CLINICAL THERMOMETER, MODELS ACT2130, ACT 2230, ACT 2330, ACT 3136, AND ACT 3030
- K021612 — DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038
- K021614 — DIGITAL CLINICAL THERMOMETER, MODEL ACT 3020
- K010238 — ACTHERM DIGITAL CLINICAL THERMOMETER, MODELS ACT2000, ACT2010, ACT2000+, ACT2010+, ACT2020+
Data sourced from openFDA. This site is unofficial and independent of the FDA.