Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AI Metrics

K-Number: K202229 · 2020-12-22

Decision Date2020-12-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AI Metrics is a medical device manufactured by Ai Metrics, LLC. It received FDA 510(k) clearance on 2020-12-22 under approval number K202229. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AI Metrics?

AI Metrics is a medical device that received FDA 510(k) clearance on 2020-12-22. It is manufactured by Ai Metrics, LLC. The 510(k) number is K202229.

When was AI Metrics approved by the FDA?

AI Metrics received FDA 510(k) clearance on 2020-12-22, under approval number K202229.

What company makes AI Metrics?

AI Metrics is manufactured by Ai Metrics, LLC.

What is the FDA product code for AI Metrics?

The FDA product code for AI Metrics is LLZ.

Related Devices (Code: LLZ)

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.