FDA 510(k)

CINA-VCF

K-Number: K240612 · 2024-05-31

Decision Date2024-05-31

Product CodeQFM

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CINA-VCF is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna.Ai. It received FDA 510(k) clearance on 2024-05-31 under 510(k) number K240612. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CINA-VCF?

CINA-VCF is a medical device that received FDA 510(k) clearance on 2024-05-31. The listed applicant is Avicenna.Ai. The 510(k) number is K240612.

When did CINA-VCF receive FDA 510(k) clearance?

CINA-VCF received FDA 510(k) clearance on 2024-05-31, under 510(k) number K240612.

Who is the listed applicant for CINA-VCF?

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-VCF?

The FDA product code for CINA-VCF is QFM.

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 K233342CINA-ASPECTS K233968CINA-iPE K221716CINA K210237CINA CHEST K200855CINA

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Related Devices (Code: QFM)

K253751CXRDetectAINeurocareai, Inc. (Dba Savelife.Ai)K252954MammoSightAINeurocareai, Inc. (Dba Savelife.Ai)K252482CogNet AI-MT+Medcognetics, Inc.K250831Annalise EnterpriseAnnalise-Ai K243808Rayvolve PTX-PEAZmed K243548BriefCase-TriageAidoc Medical , Ltd.

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.