meddevicedb.com FDA Device Reference

CARDIACINDEX COMPUTER MODEL SP 1435

K802476 Class II Traditional
Decision Date
1980-11-19
Sponsor / Applicant
Gould, Inc.

Technical Specification

510(k) Submission ID K802476
Product Code DXG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1435
Decision Date 1980-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIACINDEX COMPUTER MODEL SP 1435 received FDA 510(k) clearance under submission number K802476, sponsored by Gould, 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 1980-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code DXG and 21 CFR 870.1435, within the Cardiovascular review panel as a Class II device.