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QUEST EXERCISE STRESS SYSTEM (QUEST), VERSION 3.52

K021097 Class II Traditional
Decision Date
2002-06-28
Sponsor / Applicant
Spacelabs Medical, Inc.

Technical Specification

510(k) Submission ID K021097
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2002-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUEST EXERCISE STRESS SYSTEM (QUEST), VERSION 3.52 received FDA 510(k) clearance under submission number K021097, sponsored by Spacelabs Medical, 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 2002-06-28.

Classification & Regulation

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