Cleared Traditional

AI-Rad Companion Brain MR

K213706 · Siemens Healthcare GmbH · Radiology

Apr 2022

Decision

142d

Days

Class 2

Risk

About This 510(k) Submission

K213706 is an FDA 510(k) clearance for the AI-Rad Companion Brain MR, a Automated Radiological Image Processing Software (Class II — Special Controls, product code QIH), submitted by Siemens Healthcare GmbH (Malvern, US). The FDA issued a Cleared decision on April 15, 2022, 142 days after receiving the submission on November 24, 2021. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number	K213706 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 24, 2021
Decision Date	April 15, 2022
Days to Decision	142 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Summary PDF

Device Classification

Product Code	QIH — Automated Radiological Image Processing Software
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 892.2050
Definition	To Provide Automated Radiological Image Processing And Analysis Tools. Software Implementing Artificial Intelligence Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Data. In These Devices, The Algorithm Training Data Typically Impacts Device Performance. Adaptive Ai Algorithms Are Not Within Scope Of This Product Code.