meddevicedb.com FDA Device Reference

CLASSIC 4-WAY ELEVATING TABLE

K912474 Class II Traditional
Decision Date
1991-09-16
Sponsor / Applicant
Continental X-Ray Corp.

Technical Specification

510(k) Submission ID K912474
Product Code IZZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1980
Decision Date 1991-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLASSIC 4-WAY ELEVATING TABLE received FDA 510(k) clearance under submission number K912474, sponsored by Continental X-Ray Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code IZZ and 21 CFR 892.1980, within the Radiology review panel as a Class II device.