meddevicedb.com FDA Device Reference

ZeTTA PACS

K241694 Class II Traditional
Decision Date
2025-01-31
Sponsor / Applicant
Tae Young Soft Co., Ltd.

Technical Specification

510(k) Submission ID K241694
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2025-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZeTTA PACS received FDA 510(k) clearance under submission number K241694, sponsored by Tae Young Soft Co., 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 2025-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.