Ezra Flash
K-Number: K242334 · 2025-01-02
Device Summary
Frequently Asked Questions
What is the Ezra Flash?
Ezra Flash is a medical device that received FDA 510(k) clearance on 2025-01-02. The listed applicant is Ezra Ai, Inc.. The 510(k) number is K242334.
When did Ezra Flash receive FDA 510(k) clearance?
Ezra Flash received FDA 510(k) clearance on 2025-01-02, under 510(k) number K242334.
Who is the listed applicant for Ezra Flash?
The FDA 510(k) record lists Ezra Ai, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ezra Flash?
The FDA product code for Ezra Flash is QIH.
Other records listing Ezra Ai, Inc. 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.
Related Devices (Code: QIH)
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.
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.