meddevicedb.com FDA Device Reference

T-WAVE ALTERNANS (TWA) ALGORITHM OPTION

K032513 Class II Traditional
Decision Date
2003-10-30
Sponsor / Applicant
Ge Medical Systems Information Technologies

Technical Specification

510(k) Submission ID K032513
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2003-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T-WAVE ALTERNANS (TWA) ALGORITHM OPTION received FDA 510(k) clearance under submission number K032513, sponsored by Ge Medical Systems Information Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.