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NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM

K931410 Class I Traditional
Decision Date
1994-02-18
Sponsor / Applicant
Novus Technologies, Inc.

Technical Specification

510(k) Submission ID K931410
Product Code LMB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2010
Decision Date 1994-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM received FDA 510(k) clearance under submission number K931410, sponsored by Novus Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code LMB and 21 CFR 892.2010, within the Radiology review panel as a Class I device.