# K021614: Digital Clinical Thermometer, Model Act 3020

- Pathway: 510(k) (Special)
- Applicant: Actherm, Inc.
- Decided: May 30, 2002 after 14 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K070028: Classic/Hypothermia, Flexible, 10-Second, Left-Right Handed, Basal, Lightweight-Probe Digital Clinical Thermometer (2007), 0 descendants of its own

## Indications for use
The Digital Clinical thermometers, Models ACT 3020’s intended use are medical devices, supplied by internal power and intended to precisely measure human boduy temperature. It can be used in the measurement of oral, axillary and rectal temperature.

Source page: https://510kreport.com/device/K021614
Methodology: https://510kreport.com/methodology