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MAC VU360 Resting ECG Analysis System

K173830 Class II Traditional
Decision Date
2018-09-18
Sponsor / Applicant
Ge Medical Systems Information Technologies, Inc.

Technical Specification

510(k) Submission ID K173830
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2018-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAC VU360 Resting ECG Analysis System received FDA 510(k) clearance under submission number K173830, sponsored by Ge Medical Systems Information Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-09-18.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.