meddevicedb.com FDA Device Reference

NOGA AUTOMATED SLEEP STUDY SCORING AND DATA MANAGEMENT SYSTEM

K070326 Class II Traditional
Decision Date
2007-05-05
Sponsor / Applicant
Widemed, Ltd.

Technical Specification

510(k) Submission ID K070326
Product Code MNR
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.2375
Decision Date 2007-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOGA AUTOMATED SLEEP STUDY SCORING AND DATA MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K070326, sponsored by Widemed, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2007-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code MNR and 21 CFR 868.2375, within the Anesthesiology review panel as a Class II device.