Cleared Traditional

K242188 - ClearRead CT CAC (FDA 510(k) Clearance)

Dec 2024
Decision
131d
Days
Class 2
Risk

K242188 is an FDA 510(k) clearance for the ClearRead CT CAC. This device is classified as a System, X-ray, Tomography, Computed (Class II - Special Controls, product code JAK).

Submitted by Riverain Technologies, Inc. (Miamisburg, US). The FDA issued a Cleared decision on December 3, 2024, 131 days after receiving the submission on July 25, 2024.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1750.

Submission Details

510(k) Number K242188 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 25, 2024
Decision Date December 03, 2024
Days to Decision 131 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code JAK - System, X-ray, Tomography, Computed
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.1750

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