# K072641: Digital Electronic Thermometer, Model: FDTH-V0-1 Thru 4.

- Pathway: 510(k) (Traditional)
- Applicant: Famidoc Technology Co., Ltd.
- Decided: Nov 1, 2007 after 44 days
- Product code: FLL (Continuous Measurement Thermometer)
- Device class: 2
- Regulation: 21 CFR 880.2910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K010238 (2001). 1 ancestor in all.
9 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010238: Actherm Digital Clinical Thermometer, Models ACT2000, ACT2010, ACT2000+, ACT2010+, ACT2020+, Actherm, Inc. (2001) Summary page 3.

## Most influential descendants
- K101387: Digital Thermometer, Models BT-A11CN, BT-A21CN, BT-A41CN (2010), 8 descendants of its own
- K132514: Kinsa Smart Thermometer (2013), 2 descendants of its own
- K203731: DT100 Digital Thermometer (2021), 1 descendant of its own
- K190990: Digital Thermometer (2019), 1 descendant of its own
- K152739: Electronic Thermometer (2016), 1 descendant of its own

## Indications for use
Famidoc Digital Clinical Thermometers are intended for the measurement and monitoring of human body temperature, by doctor or consumers in the hospital or home. It is used alone for human beings at all ages.

Source page: https://510kreport.com/device/K072641
Methodology: https://510kreport.com/methodology