# K070491: Digital Forehead Thermometer, Model# KD-2200

- Pathway: 510(k) (Abbreviated)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Jun 21, 2007 after 121 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: 3 generations back to K902624 (1990). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032362: UP-Grade Forehead Thermometer, Medisim, Ltd. (2003) Summary page 1.

## Most influential descendants
- K103617: Digital Forehead Thermometer (2011), 0 descendants of its own

## Indications for use
The Digital Forehead Thermometer, Model KD-2200 is intended to measure the human body temperature using the forehead as measurement site. It can be used with adult or pediatric patients.

Source page: https://510kreport.com/device/K070491
Methodology: https://510kreport.com/methodology