meddevicedb.com FDA Device Reference

TREATMENT TABLE MODIFICATION

K936303 Class I Traditional
Decision Date
1994-03-18
Sponsor / Applicant
Tri W-G, Inc.

Technical Specification

510(k) Submission ID K936303
Product Code INQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3760
Decision Date 1994-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TREATMENT TABLE MODIFICATION received FDA 510(k) clearance under submission number K936303, sponsored by Tri W-G, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1994-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.