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FDA 510(k)

Ezra Flash

K-Number: K242334 · 2025-01-02

ApplicantEzra Ai, Inc.
Decision Date2025-01-02
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ezra Flash is a medical device manufactured by Ezra Ai, Inc.. It received FDA 510(k) clearance on 2025-01-02 under approval number K242334. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ezra Flash?

Ezra Flash is a medical device that received FDA 510(k) clearance on 2025-01-02. It is manufactured by Ezra Ai, Inc.. The 510(k) number is K242334.

When was Ezra Flash approved by the FDA?

Ezra Flash received FDA 510(k) clearance on 2025-01-02, under approval number K242334.

What company makes Ezra Flash?

Ezra Flash is manufactured by Ezra Ai, Inc..

What is the FDA product code for Ezra Flash?

The FDA product code for Ezra Flash is QIH.

Other Devices by Ezra Ai, Inc.

K192969Ezra Plexo Software K230264Ezra Flash

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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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