ClearRead CT CAC— 510(k) K242188

Name: FDA 510(k) clearance K242188
Creator: U.S. Food and Drug Administration
Published: 2024-12-03

Substantially Equivalent

Riverain Technologies, Inc.

FDA 510(k) clearance K242188 for ClearRead CT CAC, Substantially Equivalent on 2024-12-03. Applicant: Riverain Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Riverain Technologies, Inc.
Product code: Code JAK
Device class: Class 2
Regulation: 21 CFR 892.1750
Advisory panel: Radiology
Date received: 2024-07-25
Decision date: 2024-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miamisburg, OH, US

Download summary PDF View on FDA.gov ↗

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More clearances from Riverain Technologies, Inc.

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K221612 — ClearRead CT2022-12-05
K213566 — ClearRead Xray Pneumothorax2022-03-10

Adverse events under product code JAK

product code JAK

Death: 27
Injury: 571
Malfunction: 779
Total: 1,377

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.