FDA 510(k)

Radify Triage

K-Number: K231871 · 2024-01-17

Decision Date2024-01-17

Product CodeQFM

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Radify Triage is the device name listed in this FDA 510(k) record. The listed applicant is Envisionit Deepai, Ltd.. It received FDA 510(k) clearance on 2024-01-17 under 510(k) number K231871. 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 Radify Triage?

Radify Triage is a medical device that received FDA 510(k) clearance on 2024-01-17. The listed applicant is Envisionit Deepai, Ltd.. The 510(k) number is K231871.

When did Radify Triage receive FDA 510(k) clearance?

Radify Triage received FDA 510(k) clearance on 2024-01-17, under 510(k) number K231871.

Who is the listed applicant for Radify Triage?

The FDA 510(k) record lists Envisionit Deepai, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Radify Triage?

The FDA product code for Radify Triage is QFM.

Related Devices (Code: QFM)

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.

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

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