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)

CINA CHEST

K-Number: K210237 · 2021-05-19

ApplicantAvicenna.Ai
Decision Date2021-05-19
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CINA CHEST is a medical device manufactured by Avicenna.Ai. It received FDA 510(k) clearance on 2021-05-19 under approval number K210237. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CINA CHEST?

CINA CHEST is a medical device that received FDA 510(k) clearance on 2021-05-19. It is manufactured by Avicenna.Ai. The 510(k) number is K210237.

When was CINA CHEST approved by the FDA?

CINA CHEST received FDA 510(k) clearance on 2021-05-19, under approval number K210237.

What company makes CINA CHEST?

CINA CHEST is manufactured by Avicenna.Ai.

What is the FDA product code for CINA CHEST?

The FDA product code for CINA CHEST is QAS.

Other Devices by Avicenna.Ai

View all 7 devices →

Related Devices (Code: QAS)

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.