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LINX NETWORKING SYSTEM

K964250 Class I Traditional
Decision Date
1996-12-18
Sponsor / Applicant
Sterling Diagnostic Imaging, Inc.

Technical Specification

510(k) Submission ID K964250
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1996-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LINX NETWORKING SYSTEM received FDA 510(k) clearance under submission number K964250, sponsored by Sterling Diagnostic Imaging, 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 1996-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code LMD and 21 CFR 892.2020, within the Radiology review panel as a Class I device.