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NOMAD SLEEP SYSTEM RECORDER, MODEL PMU800

K092699 Class II Traditional
Decision Date
2010-03-18
Sponsor / Applicant
Neurotronics, Inc.

Technical Specification

510(k) Submission ID K092699
Product Code GWL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1835
Decision Date 2010-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOMAD SLEEP SYSTEM RECORDER, MODEL PMU800 received FDA 510(k) clearance under submission number K092699, sponsored by Neurotronics, 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 2010-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code GWL and 21 CFR 882.1835, within the Neurology review panel as a Class II device.