meddevicedb.com FDA Device Reference

BX-200 SC

K943185 Class II Traditional
Decision Date
1995-08-14
Sponsor / Applicant
Bloomex International, Inc.

Technical Specification

510(k) Submission ID K943185
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1995-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BX-200 SC received FDA 510(k) clearance under submission number K943185, 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 1995-08-14.

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.