meddevicedb.com FDA Device Reference

TREATMENT TABLE

K910838 Class II Traditional
Decision Date
1991-08-07
Sponsor / Applicant
Tri W-G, Inc.

Technical Specification

510(k) Submission ID K910838
Product Code IXR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1980
Decision Date 1991-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TREATMENT TABLE received FDA 510(k) clearance under submission number K910838, sponsored by Tri W-G, 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 1991-08-07.

Classification & Regulation

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