meddevicedb.com FDA Device Reference

IMNET DICOM NETWORK AGENT

K972366 Class I Traditional
Decision Date
1997-09-23
Sponsor / Applicant
Imnet Systems, Inc.

Technical Specification

510(k) Submission ID K972366
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1997-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMNET DICOM NETWORK AGENT received FDA 510(k) clearance under submission number K972366, sponsored by Imnet Systems, 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 1997-09-23.

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.