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PCM DIGITAL AMBULA TORY ECG ANALYSIS SYSTEM

K852968 Class II Traditional
Decision Date
1985-11-14
Sponsor / Applicant
Personal Computers For Medicine, Inc.

Technical Specification

510(k) Submission ID K852968
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1985-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PCM DIGITAL AMBULA TORY ECG ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K852968, sponsored by Personal Computers For Medicine, 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 1985-11-14.

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.