syngo Dynamics (Version VA41D)— 510(k) K242551

Name: FDA 510(k) clearance K242551
Creator: U.S. Food and Drug Administration
Published: 2025-04-03

Substantially Equivalent

Siemens Healthcare GmbH

FDA 510(k) clearance K242551 for syngo Dynamics (Version VA41D), Substantially Equivalent on 2025-04-03. Applicant: Siemens Healthcare GmbH. Device class: 2.

Clearance details

Applicant: Siemens Healthcare GmbH
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2024-08-27
Decision date: 2025-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erlanger, DE

Download summary PDF View on FDA.gov ↗

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