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ELECTRO-NERVE STIMULATOR TENS MODEL B5/SKN

K871125 Class II Traditional
Decision Date
1987-06-02
Sponsor / Applicant
Biomedical Life Systems, Inc.

Technical Specification

510(k) Submission ID K871125
Product Code GZJ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 1987-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRO-NERVE STIMULATOR TENS MODEL B5/SKN received FDA 510(k) clearance under submission number K871125, 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 1987-06-02.

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.