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HHF1 MAGNETIC RESONANCE IMAGING SYSTEM

K052172 Class II Abbreviated
Decision Date
2005-09-27
Sponsor / Applicant
Hitachi Medical Systems America, Inc.

Technical Specification

510(k) Submission ID K052172
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2005-09-27
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HHF1 MAGNETIC RESONANCE IMAGING SYSTEM received FDA 510(k) clearance under submission number K052172, 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 2005-09-27.

Classification & Regulation

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