meddevicedb.com FDA Device Reference

M1765A ECG MANAGER

K974746 Class II Traditional
Decision Date
1998-03-18
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K974746
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1998-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

M1765A ECG MANAGER received FDA 510(k) clearance under submission number K974746, sponsored by Hewlett-Packard Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-03-18.

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.