# K030324: Radiant Innovation Inc. Infrared Ear Thermometer, Models TH1 Series

- Pathway: 510(k) (Special)
- Applicant: Radiant Innovation, Inc.
- Decided: Feb 27, 2003 after 27 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 K011059 (2001). 1 ancestor in all.
21 later devices descend from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011059: Infared Ear Thermometer, Model TH8 Series, Radiant Innovation, Inc. (2001)

## Most influential descendants
- K040377: Rii Infrared Ear Thermometer, Models Thxxn Series (2004), 20 descendants of its own
- K051269: Rii Infrared Ear Thermometer, Models TH00XY Series (2005), 19 descendants of its own
- K063185: Rii Infrared Ear Thermometer, Models TH5XY Series (2006), 18 descendants of its own
- K162083: RII Multi-function Infrared Thermometer, Model TH52Z (2017), 14 descendants of its own
- K191570: Infrared Thermometer Model MD-H30 (2019), 8 descendants of its own

## Indications for use
The device is an electronic clinical thermometer using an infrared sensor to detect body temperature from the auditory canal in the neonatal, pediatric and adult population used in the home setting.

Source page: https://510kreport.com/device/K030324
Methodology: https://510kreport.com/methodology