meddevicedb.com FDA Device Reference

EMS-250

K934556 Class II Traditional
Decision Date
1994-11-08
Sponsor / Applicant
Electronic Medical Sciences, Inc.

Technical Specification

510(k) Submission ID K934556
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1994-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMS-250 received FDA 510(k) clearance under submission number K934556, sponsored by Electronic Medical Sciences, 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 1994-11-08.

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.