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BIS PEDIATRIC SENSOR

K041670 Class II Special
Decision Date
2004-07-06
Sponsor / Applicant
Aspect Medical Systems, Inc.

Technical Specification

510(k) Submission ID K041670
Product Code GXY
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1320
Decision Date 2004-07-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIS PEDIATRIC SENSOR received FDA 510(k) clearance under submission number K041670, sponsored by Aspect Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2004-07-06.

Classification & Regulation

This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.