# K014063: Task Force Monitor 3040

- Pathway: 510(k) (Traditional)
- Applicant: Cnsystems Medizintechnik GmbH
- Decided: Feb 7, 2002 after 58 days
- Product code: DSB (Plethysmograph, Impedance)
- Device class: 2
- Regulation: 21 CFR 870.2770
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K880572 (1988). 2 ancestors in all.
106 later devices descend from it; 4 cite it directly.
1 of 109 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001081: Bioz.PC Hemodynamic Monitor Model BZ-500/BZ-501; Bioz.PC User Software Installation Kit Model BZ-810, Cardiodynamics International Corp. (2000) Summary page 4.
- K880572: Ohmeda 2350 Finapres (R) Blood Pressure Monitor, Ohmeda Medical (1988) Summary page 4.

## Most influential descendants
- K023723: Finometer Noninvasive Hemodynamic Monitor, Model 1 (2003), 81 descendants of its own
- K072049: Continuous Non-Invasive Cardiac Output and Blood Pressure Monitor with Real-Time Hemodynamics (2007), 78 descendants of its own
- K101123: Nexfin Model 2 (2010), 54 descendants of its own
- K122381: Nexfin Model 2 (2013), 53 descendants of its own
- K140312: EV1000 Clinical Platform with Clearsight TM Finger Cuff or Clearsight TM System (2014), 52 descendants of its own

## Recalls of this device
- Dec 1, 2015 · Class II · Z-0572-2016: Device non-conformity which may lead to an incorrect oscillometric measurement of upper arm blood pressure values in some subjects - mainly in tall and slim persons (overestimation of systolic blood p

## Indications for use
The Task Force@Monitor 3040 (TFM) is intended to noninvasively measure and display a patient's hemodynamic parameters using Impedance Cardiography (ICG), Electrocardiography (ECG), oscillometric Blood Pressure (oscBP) and continuous Blood Pressure (contBP). The TFM monitors continuously the subject's hemodynamic parameters without reporting any diagnosis. Every measurement must be supervised by a medical trained professional. The Task Force@Monitol 3040 is a diagnosesaiding device and therefore not designed for vital sign monitoring or self-monitoring of patients.

Source page: https://510kreport.com/device/K014063
Methodology: https://510kreport.com/methodology