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ECHELON MR-RCC-150 CARDIAC COIL

K063513 Class II Abbreviated
Decision Date
2006-12-12
Sponsor / Applicant
Hitachi Medical Systems America, Inc.

Technical Specification

510(k) Submission ID K063513
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2006-12-12
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECHELON MR-RCC-150 CARDIAC COIL received FDA 510(k) clearance under submission number K063513, sponsored by Hitachi Medical Systems America, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.