LARALAB— 510(k) K242500

Substantially Equivalent

Laralab GmbH

FDA 510(k) clearance K242500 for LARALAB, Substantially Equivalent on 2025-04-16. Applicant: Laralab GmbH. Device class: 2.

Clearance details

Applicant: Laralab GmbH
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2024-08-22
Decision date: 2025-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Munich, 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.