meddevicedb.com FDA Device Reference

IDS4 IMAGE DISPLAY SYSTEM SERIES

K971368 Class II Traditional
Decision Date
1997-06-26
Sponsor / Applicant
O Tech, Inc.

Technical Specification

510(k) Submission ID K971368
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1997-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IDS4 IMAGE DISPLAY SYSTEM SERIES received FDA 510(k) clearance under submission number K971368, sponsored by O Tech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-06-26.

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.