# K040562: Lifeclinic, Model 2400

- Pathway: 510(k) (Special)
- Applicant: Lifeclinic International, Inc.
- Decided: Aug 31, 2004 after 181 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- 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 K850893 (1985). 1 ancestor in all.
8 later devices descend from it; 4 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K850893: BP/Clinic Sys Measurement, BP Non-Invasive, Sun Dance Technology, Inc. (1985) Summary page 1.

## Most influential descendants
- K063137: Pharmasmart Public Use Blood Pressure Monitor, Models PS-1000/PS-1500/PS-2000 (2007), 5 descendants of its own
- K063008: Health Check Kiosk (2007), 4 descendants of its own
- K093389: Csi Model 5K Managed Health System Kiosk (2009), 3 descendants of its own
- K101198: Csi Managed Health System Model: Csi Model 9K (2010), 1 descendant of its own
- K153600: Consult Station TS (2017), 0 descendants of its own

## Indications for use
The Lifeclinic LC500 is indicated for the measurement of blood pressure and heart rate by members of the general public. The device does not perform any diagnoses; it only provides pressure and rate data to the users, who are advised to consult a physician.

Source page: https://510kreport.com/device/K040562
Methodology: https://510kreport.com/methodology