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SLEEP STUDY ANALYSIS (SSA) VERSION 96.10

K963631 Class II Traditional
Decision Date
1997-04-02
Sponsor / Applicant
Omega Results

Technical Specification

510(k) Submission ID K963631
Product Code OLZ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 1997-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLEEP STUDY ANALYSIS (SSA) VERSION 96.10 received FDA 510(k) clearance under submission number K963631, sponsored by Omega Results. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1997-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code OLZ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.