meddevicedb.com FDA Device Reference

Optical Topography System ETG-4100

K172492 Class II Traditional
Decision Date
2018-08-17
Sponsor / Applicant
Hitachi Healthcare Americas

Technical Specification

510(k) Submission ID K172492
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2018-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Optical Topography System ETG-4100 received FDA 510(k) clearance under submission number K172492, sponsored by Hitachi Healthcare Americas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-08-17.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.