meddevicedb.com FDA Device Reference

HEART-EXERCISE

K091594 Class II Traditional
Decision Date
2009-07-29
Sponsor / Applicant
Ge Medical Systems Information Technologies GmbH

Technical Specification

510(k) Submission ID K091594
Product Code MHX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2009-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEART-EXERCISE received FDA 510(k) clearance under submission number K091594, sponsored by Ge Medical Systems Information Technologies GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-07-29.

Classification & Regulation

This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.