meddevicedb.com FDA Device Reference

PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601

K032038 Class II Abbreviated
Decision Date
2003-09-05
Sponsor / Applicant
Quinton, Inc.

Technical Specification

510(k) Submission ID K032038
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2003-09-05
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601 received FDA 510(k) clearance under submission number K032038, sponsored by Quinton, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-09-05.

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.