meddevicedb.com FDA Device Reference

BMLS03-3

K033174 Class II Traditional
Decision Date
2004-06-30
Sponsor / Applicant
Biomedical Life Systems, Inc.

Technical Specification

510(k) Submission ID K033174
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2004-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BMLS03-3 received FDA 510(k) clearance under submission number K033174, sponsored by Biomedical Life Systems, 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 2004-06-30.

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.