meddevicedb.com FDA Device Reference

HealthICH

K190424 Class II Traditional
Decision Date
2019-06-13
Sponsor / Applicant
Zebra Medical Vision, Ltd.

Technical Specification

510(k) Submission ID K190424
Product Code QAS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2080
Decision Date 2019-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HealthICH received FDA 510(k) clearance under submission number K190424, sponsored by Zebra Medical Vision, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2019-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code QAS and 21 CFR 892.2080, within the Radiology review panel as a Class II device.