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COR ANALYZER

K110071 Class II Special
Decision Date
2011-01-31
Sponsor / Applicant
Rcadia Medical Imaging , Ltd.

Technical Specification

510(k) Submission ID K110071
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2011-01-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COR ANALYZER received FDA 510(k) clearance under submission number K110071, sponsored by Rcadia Medical Imaging , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-01-31.

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.