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IMIX INSIGHT X-RAY SYSTEMS

K073114 Class II Special
Decision Date
2008-01-17
Sponsor / Applicant
Imix Adr Finland OY

Technical Specification

510(k) Submission ID K073114
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2008-01-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMIX INSIGHT X-RAY SYSTEMS received FDA 510(k) clearance under submission number K073114, sponsored by Imix Adr Finland OY. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.