Digital Clinical Thermometer, Models ACT2130, Act 2230, Act 2330, Act 3136, and Act 3030

FDA 510(k) K031905 · Actherm, Inc.

Substantially Equivalent

510(k) numberK031905

Submission

Device name
Digital Clinical Thermometer, Models ACT2130, Act 2230, Act 2330, Act 3136, and Act 3030
Applicant
Actherm, Inc.
Hsinchu, TW
Received
June 20, 2003
Decision date
July 7, 2003
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FLL – Continuous Measurement Thermometer
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2910
Specialty
General Hospital

A continuous measurement thermometer is a clinical electronic thermometer indicated to measure the body or skin temperature of a person continuously or in specified intervals. Under this regulation, this product code represents non-exempt devices. For more information, see 90 FR 25889, available at https://www.govinfo.gov/content/pkg/FR-2025-06-18/pdf/2025-11207.pdf.

Other 510(k)s with product code FLL

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K253162Temperature probes (T2252-PG); Temperature probes (TCMA-AG); Temperature probes…FLL · Traditional Unimed Medical Supplies, Inc.06/05/2026SE
K251160Sterile temperature probe (Model: W0001ES, W0028ES, W0101FS-A, W0101FS-P, W0099LS…FLL · Traditional Shenzhen Med-Link Electronics Tech Co., Ltd.01/08/2026SE
K250470Ear Thermometer (EAR-E101); Ear Thermometer (EAR-E102); Ear Thermometer (EAR-E103)FLL · Traditional Shenzhen AOJ Medical Technology Co., Ltd.06/23/2025SE
K243000Reusable Temperature Probe (T1306, T2306, T3306, T4306); Disposable Temperature Probe…FLL · Traditional Shenzhen Medke Technology Co., Ltd.06/20/2025SE
K250878YUWELL® Infrared Ear Thermometer (YHT100); YUWELL® Infrared Ear Thermometer (YHT107)FLL · Traditional Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.05/22/2025SE
K243082Infrared ThermometerFLL · Traditional Guangzhou Daxin Health Technology Co., Ltd.04/25/2025SE
K250401AION TempShield™FLL · Traditional Aion Biosystems, Inc.03/14/2025SE
K243136Non-contact Forehead Infrared Thermometer (FC-IR2000, FC-IR205, FC-IR202, FC-IR206…FLL · Traditional Shenzhen Finicare Co., Ltd.02/14/2025SE
K240333Wearable Digital Thermometer (T31)FLL · Traditional Guangdong Genial Technology Co., Ltd.10/30/2024SE
K240223FMT Disposable and Autoclavable Temperature ProbesFLL · Traditional Metko Medikal VE Tibbi Cihazlar Dis Ticaret…10/25/2024SE

More from Metko Medikal VE Tibbi Cihazlar Dis Ticaret Limited Sirketi

510(k)DeviceDecision
K093795Actherm Infrared Ear Thermometer Act 8000R Series and Its Probe Cover Med ACCU2010FLL · Special 03/12/2010SE
K083419Actherm Digital Clinical Thermometer Probe Covers, Model(S) MEDACCU1010, MEDACCU1010-1…FLL · Traditional 07/16/2009SE
K090031Actherm Infrared Ear Thermometer, Act 8000 Series; Probe Cover for Actherm Infrared Ear…FLL · Traditional 04/16/2009SE
K070028Classic/Hypothermia, Flexible, 10-SECOND, Left-Right Handed, Basal, Lightweight-Probe…FLL · Special 02/08/2007SE
K021614Digital Clinical Thermometer, Model Act 3020FLL · Special 05/30/2002SE
K021612Digital Clinical Thermometer, Models Act 2030, 2038FLL · Special 05/30/2002SE
K010238Actherm Digital Clinical Thermometer, Models ACT2000, ACT2010, ACT2000+, ACT2010+…FLL · Traditional 02/06/2001SE

Questions and answers

When was Digital Clinical Thermometer, Models ACT2130, Act 2230, Act 2330, Act 3136, and Act 3030 cleared by the FDA?

Digital Clinical Thermometer, Models ACT2130, Act 2230, Act 2330, Act 3136, and Act 3030 (K031905) received a 510(k) decision of Substantially Equivalent on July 7, 2003, 17 days after the submission was received.

What is the product code of K031905?

The FDA product code is FLL – Continuous Measurement Thermometer, a Class II (moderate risk) device regulated under 21 CFR 880.2910.