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PC BASED ELECTROCARDIOGRAPH SYSTEM (PC-ECG)

K963578 Class II Traditional
Decision Date
1997-06-30
Sponsor / Applicant
Intl. Products, Inc.

Technical Specification

510(k) Submission ID K963578
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1997-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PC BASED ELECTROCARDIOGRAPH SYSTEM (PC-ECG) received FDA 510(k) clearance under submission number K963578, sponsored by Intl. Products, 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 1997-06-30.

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.