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SOMATOM EMOTION 6 CT SYSTEMS, SOMATOM EMOTION 16

K133424 Class II Special
Decision Date
2014-01-17
Sponsor / Applicant
Siemens Medical Solutions USA, Inc.

Technical Specification

510(k) Submission ID K133424
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2014-01-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOMATOM EMOTION 6 CT SYSTEMS, SOMATOM EMOTION 16 received FDA 510(k) clearance under submission number K133424, sponsored by Siemens Medical Solutions USA, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.