# K003313: Filac Fas Temp Electronic Thermometer

- Pathway: 510(k) (Traditional)
- Applicant: The Kendall Company
- Decided: Jan 11, 2001 after 80 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
No predicates in its family tree.
7 later devices descend from it; 4 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K153135: Vital Signs Monitor (2016), 2 descendants of its own
- K131818: Vital Signs Monitor (2013), 1 descendant of its own
- K200434: V20, V20a, AVSM3 SNF (2020), 0 descendants of its own
- K181919: Patient Monitor (2019), 0 descendants of its own
- K180380: vital signs monitor (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K003313
Methodology: https://510kreport.com/methodology