meddevicedb.com FDA Device Reference

LARGE SCREEN CRT DISPLAY #1311B

K801000 Class II Traditional
Decision Date
1980-05-28
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K801000
Product Code DXJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2450
Decision Date 1980-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LARGE SCREEN CRT DISPLAY #1311B received FDA 510(k) clearance under submission number K801000, 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 1980-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code DXJ and 21 CFR 870.2450, within the Cardiovascular review panel as a Class II device.