meddevicedb.com FDA Device Reference

ZARGIS ACOUSTIC CARDIOSCAN

K031517 Class II Traditional
Decision Date
2004-05-26
Sponsor / Applicant
Zargis Medical Corp.

Technical Specification

510(k) Submission ID K031517
Product Code DQD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1875
Decision Date 2004-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZARGIS ACOUSTIC CARDIOSCAN received FDA 510(k) clearance under submission number K031517, sponsored by Zargis Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code DQD and 21 CFR 870.1875, within the Cardiovascular review panel as a Class II device.