meddevicedb.com FDA Device Reference

ASCENTIA HEARTSTATION ECG MANAGEMENT SYSTEM

K050858 Class II Abbreviated
Decision Date
2005-06-29
Sponsor / Applicant
Heartlab, Inc.

Technical Specification

510(k) Submission ID K050858
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2005-06-29
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASCENTIA HEARTSTATION ECG MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K050858, sponsored by Heartlab, 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 2005-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.