meddevicedb.com FDA Device Reference

Automatic Anatomy Recognition (AAR)

K203610 Class II Traditional
Decision Date
2021-04-20
Sponsor / Applicant
Quantitative Radiology Solutions, LLC

Technical Specification

510(k) Submission ID K203610
Product Code QKB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2021-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Automatic Anatomy Recognition (AAR) received FDA 510(k) clearance under submission number K203610, sponsored by Quantitative Radiology Solutions, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2021-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code QKB and 21 CFR 892.2050, within the Radiology review panel as a Class II device.