# K223332: Task Force CORE

- Pathway: 510(k) (Traditional)
- Applicant: Cnsystems Medizintechnik GmbH
- Decided: Apr 12, 2023 after 163 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: 12 generations back to K000126 (2000). 105 ancestors in all.
No later device cites it as a predicate yet.
5 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173916: Finapres Nova Noninvasive Hemodynamic Monitor, Finapres Medical Systems B.V. (2018) Summary page 5.
- K183521: CNAP Monitor, Cnsystems Medizintechnik GmbH (2019) Summary page 5.

## Indications for use
The Task Force® CORE (TFC) is intended for the measurement of non-invasive continuous blood pressure, pulse rate, and the determination of associated derived hemodynamic parameters. The TFC is intended to be used in professional healthcare facilities and operated by qualified healthcare professional staff. The TFC is intended to be used for adults and under uninterrupted surveillance of the operator. The TFC contains software which runs on a separate computer and which is used to operate the device. This software includes a basic frontend (Task Force® CORE Viewer) as well as an interface for integration into other software products. The TFC can provide all signals as well as measured and derived parameters to the analog output interface and can acquire signals from the analog input interface.

Source page: https://510kreport.com/device/K223332
Methodology: https://510kreport.com/methodology