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PAGE-WRITER INTERPRETIVE CARDIOGRAPH

K842370 Class II Traditional
Decision Date
1984-12-07
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K842370
Product Code DXH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2920
Decision Date 1984-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAGE-WRITER INTERPRETIVE CARDIOGRAPH received FDA 510(k) clearance under submission number K842370, 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 1984-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.