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ELTRAX OPTICAL DISK IMAGE ARCHIVING SYSTEM

K923680 Class I Traditional
Decision Date
1992-10-20
Sponsor / Applicant
Minnetonka Medical

Technical Specification

510(k) Submission ID K923680
Product Code LMB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2010
Decision Date 1992-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELTRAX OPTICAL DISK IMAGE ARCHIVING SYSTEM received FDA 510(k) clearance under submission number K923680, sponsored by Minnetonka Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-10-20.

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.