meddevicedb.com FDA Device Reference

2000 X-RAY - TOMOGRAPHIC

K931815 Class II Traditional
Decision Date
1993-08-23
Sponsor / Applicant
Imaging Sciences Intl., Inc.

Technical Specification

510(k) Submission ID K931815
Product Code IZF
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1740
Decision Date 1993-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

2000 X-RAY - TOMOGRAPHIC received FDA 510(k) clearance under submission number K931815, sponsored by Imaging Sciences Intl., 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 1993-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code IZF and 21 CFR 892.1740, within the Radiology review panel as a Class II device.