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REDI-VU SYSTEMS (SEND & RECEIVE)

K954008 Class I Traditional
Decision Date
1995-10-27
Sponsor / Applicant
Jd Technical Services, Inc.

Technical Specification

510(k) Submission ID K954008
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1995-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REDI-VU SYSTEMS (SEND & RECEIVE) received FDA 510(k) clearance under submission number K954008, sponsored by Jd Technical Services, 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 1995-10-27.

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.