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INTERFERENTIAL STIMULATOR, MODEL BMLS02-6

K040007 Class II Traditional
Decision Date
2004-07-07
Sponsor / Applicant
Biomedical Life Systems, Inc.

Technical Specification

510(k) Submission ID K040007
Product Code LIH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2004-07-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERFERENTIAL STIMULATOR, MODEL BMLS02-6 received FDA 510(k) clearance under submission number K040007, sponsored by Biomedical Life Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2004-07-07.

Classification & Regulation

This clearance is catalogued under FDA product code LIH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.