meddevicedb.com FDA Device Reference

EF2000

K820953 Class II Traditional
Decision Date
1982-07-22
Sponsor / Applicant
Squire, Sanders & Dempsey

Technical Specification

510(k) Submission ID K820953
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1982-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EF2000 received FDA 510(k) clearance under submission number K820953, sponsored by Squire, Sanders & Dempsey. 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 1982-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.