# K102135: Vector Event Grid Architecture (Vega) System

- Pathway: 510(k) (Traditional)
- Applicant: Nuvon, Inc.
- Decided: Oct 22, 2010 after 85 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K000635 (2000). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032142: Datacaptor, Capsule Technologie (2003) Summary page 5.

## Indications for use
The Vector Event Grid Architecture System is intended for use in data collection from bedside and point of care biomedical devices and clinical information management systems either directly or through networks with independent bedside devices. The Vector Event Grid Architecture System is not intended for monitoring purposes, nor is it intended to control any of the biomedical devices and information systems with which it interconnects.

Source page: https://510kreport.com/device/K102135
Methodology: https://510kreport.com/methodology