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FDA 510(k)

Automatic Anatomy Recognition (AAR)

K-Number: K203610 · 2021-04-20

ApplicantQuantitative Radiology Solutions, LLC
Decision Date2021-04-20
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Automatic Anatomy Recognition (AAR) is a medical device manufactured by Quantitative Radiology Solutions, LLC. It received FDA 510(k) clearance on 2021-04-20 under approval number K203610. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Automatic Anatomy Recognition (AAR)?

Automatic Anatomy Recognition (AAR) is a medical device that received FDA 510(k) clearance on 2021-04-20. It is manufactured by Quantitative Radiology Solutions, LLC. The 510(k) number is K203610.

When was Automatic Anatomy Recognition (AAR) approved by the FDA?

Automatic Anatomy Recognition (AAR) received FDA 510(k) clearance on 2021-04-20, under approval number K203610.

What company makes Automatic Anatomy Recognition (AAR)?

Automatic Anatomy Recognition (AAR) is manufactured by Quantitative Radiology Solutions, LLC.

What is the FDA product code for Automatic Anatomy Recognition (AAR)?

The FDA product code for Automatic Anatomy Recognition (AAR) is QKB.

Related PubMed Literature

PMID: 40407411 A data augmentation approach for an automatic speech recognition system using laser Doppler vibrometer technology. JASA express letters (2025)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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