meddevicedb.com FDA Device Reference

9600 FLUOROSCOPIC IMAGING SYSTEM

K926056 Class II Traditional
Decision Date
1993-01-21
Sponsor / Applicant
Oec-Diasonics, Inc.

Technical Specification

510(k) Submission ID K926056
Product Code OXO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1993-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

9600 FLUOROSCOPIC IMAGING SYSTEM received FDA 510(k) clearance under submission number K926056, sponsored by Oec-Diasonics, 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 1993-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.