meddevicedb.com FDA Device Reference

KIMAX REMOTE VIEWING STATION

K013098 Class II Traditional
Decision Date
2001-12-07
Sponsor / Applicant
Medical Metrics, Inc.

Technical Specification

510(k) Submission ID K013098
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2001-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KIMAX REMOTE VIEWING STATION received FDA 510(k) clearance under submission number K013098, sponsored by Medical Metrics, 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 2001-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.