# K131048: Lidco Cnap Module

- Pathway: 510(k) (Traditional)
- Applicant: Lidco, Ltd.
- Decided: Aug 28, 2013 after 135 days
- Product code: DXG (Computer, Diagnostic, Pre-Programmed, Single-Function)
- Device class: 2
- Regulation: 21 CFR 870.1435
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The LiDCO CNAP Module Is Indicated for the continuous, non-Invasive monitoring of arterial blood pressure In adults and pediatric patients from the age of 4 years by medical professionals. The LiDCO CNAP Module Is intended to be used with, and display on, the LiDCOrapid V2 Monitor. The LiDCO CNAP Module supports the following parameters: Continuous and oscillometric arterial blood pressure Arterial systolic pressure Arterial diastolic pressure Arterial mean pressure Heart rate Locations of Use: Suitable patients will be receiving treatment In the following areas: Medical and Surgical Intensive Care Units Operative Suites Step Down / High Dependency Units Trauma / Accident & Emergency Departments Coronary Intensive Care Units Cardiac Catheter Laboratories

Source page: https://510kreport.com/device/K131048
Methodology: https://510kreport.com/methodology