meddevicedb.com FDA Device Reference

BX-600 EMS

K832976 Class II Traditional
Decision Date
1983-11-25
Sponsor / Applicant
Bloomex International, Inc.

Technical Specification

510(k) Submission ID K832976
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1983-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BX-600 EMS received FDA 510(k) clearance under submission number K832976, sponsored by Bloomex International, 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 1983-11-25.

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.