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SYNGO.CT CORONARY ANALYSIS

K100637 Class II Traditional
Decision Date
2010-05-26
Sponsor / Applicant
Siemens AG Medical Solutions

Technical Specification

510(k) Submission ID K100637
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2010-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNGO.CT CORONARY ANALYSIS received FDA 510(k) clearance under submission number K100637, sponsored by Siemens AG Medical Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2010-05-26.

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.