Ceevra Reveal 3+

FDA 510(k) K243933 · Ceevra, Inc.

Substantially Equivalent

510(k) numberK243933

Submission

Device name
Ceevra Reveal 3+
Applicant
Ceevra, Inc.
San Francisco, CA, US
Received
December 20, 2024
Decision date
March 4, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QIH – Automated Radiological Image Processing Software
Device class
Class II (moderate risk)
Regulation
21 CFR 892.2050
Specialty
Radiology

To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the algorithm training data typically impacts device performance. Adaptive AI algorithms are not within scope of this product code.

Other 510(k)s with product code QIH

510(k)DeviceApplicantDecision
K261795Quicktome Software SuiteQIH · Traditional Omniscient Neurotechnology Pty, Ltd.09/10/2026SE
K2608794DMQIH · Traditional Invia, LLC09/10/2026SE
K251417ReVISION 2QIH · Traditional Argus Cognitive, Inc.09/09/2026SE
K260525NextMR SpineQIH · Traditional MRI2CT, Inc.09/04/2026SE
K260811Heartvue.ProtonQIH · Traditional Heartvue.ai, Inc.08/26/2026SE
K261595Ceevra Reveal 4QIH · Traditional Ceevra, Inc.08/25/2026SE
K262127DS Core CBCT AnatomyQIH · Traditional Dentsply Sirona08/21/2026SE
K260584BoneMRIQIH · Traditional Mriguidance B.V.08/21/2026SE
K261641Lower Limb AI (LLAI)QIH · Traditional AI Planning Logic, Inc.08/18/2026SE
K253794Prostate CoreQIH · Traditional Lucida Medical, Ltd.08/10/2026SE

More from Lucida Medical, Ltd.

510(k)DeviceDecision
K261595Ceevra Reveal 4QIH · Traditional 08/25/2026SE
K233568Ceevra Reveal 3+QIH · Special 12/05/2023SE
K222676Ceevra Reveal 3QIH · Traditional 04/25/2023SE
K173274Ceevra Reveal 2.0LLZ · Traditional 07/10/2018SE
K171356Clarity RevealLLZ · Traditional 08/03/2017SE

Questions and answers

When was Ceevra Reveal 3+ cleared by the FDA?

Ceevra Reveal 3+ (K243933) received a 510(k) decision of Substantially Equivalent on March 4, 2025, 74 days after the submission was received.

What is the product code of K243933?

The FDA product code is QIH – Automated Radiological Image Processing Software, a Class II (moderate risk) device regulated under 21 CFR 892.2050.