meddevicedb.com FDA Device Reference

ELECTRO-NERVE STIMULATOR DISCO B9 TENS

K851191 Class II Traditional
Decision Date
1985-05-31
Sponsor / Applicant
Biomedical Life Systems, Inc.

Technical Specification

510(k) Submission ID K851191
Product Code GZJ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 1985-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRO-NERVE STIMULATOR DISCO B9 TENS received FDA 510(k) clearance under submission number K851191, 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 1985-05-31.

Classification & Regulation

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