# K082599: Non-Invasive Continuous Blood Pressure Monitoring System Cnap Monitor 500I, 500AT

- Pathway: 510(k) (Traditional)
- Applicant: Cnsystem Medizintechnik AG
- Decided: Oct 17, 2008 after 39 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: 6 generations back to K962603 (1997). 13 ancestors in all.
25 later devices descend from it; 3 cite it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014063: Task Force Monitor 3040, Cnsystems Medizintechnik GmbH (2002) Summary page 1.
- K032363: Zoll M Series Nibp Option, Zoll Medical Corp (2003) Summary page 1.

## Most influential descendants
- K130709: Visi Mobile Monitoring System (2013), 19 descendants of its own
- K143751: Visi Mobile Monitoring System (2015), 17 descendants of its own
- K150992: Vios Monitoring System (2015), 7 descendants of its own
- K150361: ViSi Mobile Monitoring System (2015), 6 descendants of its own
- K183067: Guardian Angel Rx GA2000 Digital Vital Sign Monitoring System (2019), 4 descendants of its own

## Indications for use
The CNAP Monitor 500 is intended for the monitoring of non-invasive continuous blood pressure and pulse rate in hospitals, clinical institutions, medical practices and outpatient settings. The device displays the blood pressure waveform and generates trends, beat-to-beat numerics and alarms for the parameters blood pressure and pulse rate. The CNAP Monitor 500 is to be used for adults and pediatric patients from the age of 4 year and is to be operated by physicians and other medical professional staff.

Source page: https://510kreport.com/device/K082599
Methodology: https://510kreport.com/methodology