meddevicedb.com FDA Device Reference

THE TRACKER

K923033 Class II Traditional
Decision Date
1993-06-01
Sponsor / Applicant
Epm Information Systems, Inc.

Technical Specification

510(k) Submission ID K923033
Product Code LXJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5360
Decision Date 1993-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE TRACKER received FDA 510(k) clearance under submission number K923033, sponsored by Epm Information Systems, 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 1993-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code LXJ and 21 CFR 890.5360, within the Physical Medicine review panel as a Class II device.