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ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE

K131045 Class II Traditional
Decision Date
2013-05-29
Sponsor / Applicant
Cardiac Designs, LLC

Technical Specification

510(k) Submission ID K131045
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2013-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE received FDA 510(k) clearance under submission number K131045, sponsored by Cardiac Designs, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-05-29.

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.