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FDA 510(k)

Radify Triage

K-Number: K231871 · 2024-01-17

ApplicantEnvisionit Deepai, Ltd.
Decision Date2024-01-17
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Radify Triage is a medical device manufactured by Envisionit Deepai, Ltd.. It received FDA 510(k) clearance on 2024-01-17 under approval 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. It is manufactured by Envisionit Deepai, Ltd.. The 510(k) number is K231871.

When was Radify Triage approved by the FDA?

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

What company makes Radify Triage?

Radify Triage is manufactured by Envisionit Deepai, Ltd..

What is the FDA product code for Radify Triage?

The FDA product code for Radify Triage is QFM.

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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.

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