meddevicedb.com FDA Device Reference

EMS/400

K913272 Class II Traditional
Decision Date
1991-08-22
Sponsor / Applicant
Altoona Medical Supply

Technical Specification

510(k) Submission ID K913272
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1991-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMS/400 received FDA 510(k) clearance under submission number K913272, sponsored by Altoona Medical Supply. 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 1991-08-22.

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.