Relu Creator— 510(k) K233925

Substantially Equivalent

Relu BV

FDA 510(k) clearance K233925 for Relu Creator, Substantially Equivalent on 2024-06-13. Applicant: Relu BV. Device class: 2.

Clearance details

Applicant: Relu BV
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2023-12-13
Decision date: 2024-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leuven, BE

Download summary PDF View on FDA.gov ↗

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