FDA 510(k)

CINA CHEST

K-Number: K210237 · 2021-05-19

Decision Date2021-05-19

Product CodeQAS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CINA CHEST is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna.Ai. It received FDA 510(k) clearance on 2021-05-19 under 510(k) 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. The listed applicant is Avicenna.Ai. The 510(k) number is K210237.

When did CINA CHEST receive FDA 510(k) clearance?

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

Who is the listed applicant for CINA CHEST?

The FDA 510(k) record lists Avicenna.Ai as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CINA CHEST?

The FDA product code for CINA CHEST is QAS.

Other records listing Avicenna.Ai as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K240942CINA-CSpine K240612CINA-VCF K233342CINA-ASPECTS K233968CINA-iPE K221716CINA K200855CINA

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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.