Ceevra Reveal 3— 510(k) K222676

Substantially Equivalent

Ceevra, Inc.

FDA 510(k) clearance K222676 for Ceevra Reveal 3, Substantially Equivalent on 2023-04-25. Applicant: Ceevra, Inc.. Device class: 2.

Clearance details

Applicant: Ceevra, Inc.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2022-09-06
Decision date: 2023-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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