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IBM 588 DIGITAL ECG ACQUISITION/ANALYSIS

K830163 Class II Traditional
Decision Date
1983-02-18
Sponsor / Applicant
Intl. Business Machines

Technical Specification

510(k) Submission ID K830163
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1983-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IBM 588 DIGITAL ECG ACQUISITION/ANALYSIS received FDA 510(k) clearance under submission number K830163, sponsored by Intl. Business Machines. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1983-02-18.

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.