Skip to content

Vector Event Grid Architecture (VEGA) System

by Nuvon, Inc.

510(k) K102135

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK102135 Date22 Oct 2010ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MWI
Device Class
Class II
Regulation
21 CFR Part 870.2300
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Vector Event Grid Architecture (VEGA) System is a software and hardware solution designed for data collection from bedside and point of care biomedical devices. It functions as an intelligent device manager that monitors and controls heterogeneous devices within a healthcare network, including clinical information management systems.

This system is supplied as a medical grade appliance intended for use by IT and clinical engineering departments. It incorporates secure parameters for managing data connectivity across healthcare environments. The device is authorized under FDA 510(k) clearance K102135.

Other devices from Nuvon, Inc.