meddevicedb.com FDA Device Reference

EXCEL TX

K940200 Class II Traditional
Decision Date
1994-06-07
Sponsor / Applicant
Excel Tech. , Ltd.

Technical Specification

510(k) Submission ID K940200
Product Code ITH
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5900
Decision Date 1994-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXCEL TX received FDA 510(k) clearance under submission number K940200, sponsored by Excel Tech. , Ltd.. 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 1994-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code ITH and 21 CFR 890.5900, within the Physical Medicine review panel as a Class II device.