meddevicedb.com FDA Device Reference

ECG ANALYZER, HIGH SPEED

K781911 Class II Traditional
Decision Date
1978-11-30
Sponsor / Applicant
Cardio-Dynamics Laboratories, Inc.

Technical Specification

510(k) Submission ID K781911
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1978-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECG ANALYZER, HIGH SPEED received FDA 510(k) clearance under submission number K781911, sponsored by Cardio-Dynamics Laboratories, 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 1978-11-30.

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.