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MAGNETOM SYMPHONY A TIM SYSTEM

K050199 Class II Traditional
Decision Date
2005-02-18
Sponsor / Applicant
Siemens Medical Solution

Technical Specification

510(k) Submission ID K050199
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2005-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGNETOM SYMPHONY A TIM SYSTEM received FDA 510(k) clearance under submission number K050199, sponsored by Siemens Medical Solution. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-02-18.

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.