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FDA 510(k)

VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM

K-Number: K102135 · 2010-10-22

ApplicantNuvon, Inc.
Decision Date2010-10-22
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvon, Inc.. It received FDA 510(k) clearance on 2010-10-22 under 510(k) number K102135. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM?

VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM is a medical device that received FDA 510(k) clearance on 2010-10-22. The listed applicant is Nuvon, Inc.. The 510(k) number is K102135.

When did VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM receive FDA 510(k) clearance?

VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM received FDA 510(k) clearance on 2010-10-22, under 510(k) number K102135.

Who is the listed applicant for VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM?

The FDA 510(k) record lists Nuvon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM?

The FDA product code for VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM is MWI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Nuvon, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K130234NUVON VITALS CHARTING SYSTEM

Related Devices (Code: MWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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