# K033967: Telethermographic Camera, Series a, E, S and P

- Pathway: 510(k) (Traditional)
- Applicant: Flir Systems
- Decided: Mar 9, 2004 after 78 days
- Product code: LHQ (System, Telethermographic (Adjunctive Use))
- Device class: 1
- Regulation: 21 CFR 884.2980
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K951806 (1995). 3 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982327: Inframetrics Infracam-Med, Inframetrics, Inc. (1998) Summary page 1.
- K023434: Dorex Spectrum 9000MB Thermography System, Dorex, Inc. (2002) Summary page 1.

## Most influential descendants
- K101641: AG Thermographic Camera, Model Atir-M301 (2011), 0 descendants of its own
- K073581: Ici P and S Series IR Cameras (2008), 0 descendants of its own

## Indications for use
The Flir devices are intended for use as an adjunct to other clinical diagnostic procedures in the diagnosis, quantifying, and screening of differences in skin surface temperature changes. It can visualize, document temperature patterns and changes. Environment of use: hospital, sub-acute, public areas, i.e., airports

Source page: https://510kreport.com/device/K033967
Methodology: https://510kreport.com/methodology