meddevicedb.com FDA Device Reference

BIOLOGIC SYSTEM BL 101

K831047 Class II Traditional
Decision Date
1983-05-13
Sponsor / Applicant
Bio-Logic Systems Corp.

Technical Specification

510(k) Submission ID K831047
Product Code GWE
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1890
Decision Date 1983-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOLOGIC SYSTEM BL 101 received FDA 510(k) clearance under submission number K831047, sponsored by Bio-Logic Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1983-05-13.

Classification & Regulation

This clearance is catalogued under FDA product code GWE and 21 CFR 882.1890, within the Neurology review panel as a Class II device.