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VISTA POLYSOMNOGRAPHY COMPUTER SYSTEM

K904328 Class II Traditional
Decision Date
1991-06-18
Sponsor / Applicant
Telediagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K904328
Product Code GWK
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1845
Decision Date 1991-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISTA POLYSOMNOGRAPHY COMPUTER SYSTEM received FDA 510(k) clearance under submission number K904328, sponsored by Telediagnostic Systems, 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 1991-06-18.

Classification & Regulation

This clearance is catalogued under FDA product code GWK and 21 CFR 882.1845, within the Neurology review panel as a Class II device.