# K102947: Non-Contact Infrared Thermometer

- Pathway: 510(k) (Traditional)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Feb 25, 2011 after 144 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: 4 generations back to K010462 (2001). 5 ancestors in all.
8 later devices descend from it; 3 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080759: Thermoflash LX-26, Jxb Co. Ltd Guangzhou (China) (2008) Summary page 1.

## Most influential descendants
- K131243: Non-Contact Infrared Thermometer (2013), 5 descendants of its own
- K160816: Infrared Thermometer (Model: LX-26E, LX-260TE, PRO LX-261E, LX-360, LX-361T, BW-CX10) (2016), 1 descendant of its own
- K210118: INFRARED BODY THERMOMETER (Model: YK-001) (2021), 0 descendants of its own
- K202111: Medical infrared forehead thermometer (2021), 0 descendants of its own
- K172889: Infrared Thermometer (2018), 0 descendants of its own

## Indications for use
Non-Contact Infrared Thermometer, Model KI-8280, can measure body temperature for infants and adults without contact to human body. It can be used by consumers in household environment and doctor in clinic as reference.

Source page: https://510kreport.com/device/K102947
Methodology: https://510kreport.com/methodology