meddevicedb.com FDA Device Reference

E-STRIP

K031769 Class II Traditional
Decision Date
2003-10-14
Sponsor / Applicant
Eemso, Inc.

Technical Specification

510(k) Submission ID K031769
Product Code EGJ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5525
Decision Date 2003-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-STRIP received FDA 510(k) clearance under submission number K031769, sponsored by Eemso, 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 2003-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code EGJ and 21 CFR 890.5525, within the Physical Medicine review panel as a Class II device.