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MILTRA IMAGING INC., IMAGE VAULT

K974102 Class I Traditional
Decision Date
1998-01-20
Sponsor / Applicant
Mitra Imaging, Inc.

Technical Specification

510(k) Submission ID K974102
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1998-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILTRA IMAGING INC., IMAGE VAULT received FDA 510(k) clearance under submission number K974102, sponsored by Mitra 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 1998-01-20.

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.