Alzevita— 510(k) K252670

Substantially Equivalent

TOPIA MEDTECH LIMITED

FDA 510(k) clearance K252670 for Alzevita, Substantially Equivalent on 2025-12-19. Applicant: TOPIA MEDTECH LIMITED. Device class: 2.

Clearance details

Applicant: TOPIA MEDTECH LIMITED
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2025-08-25
Decision date: 2025-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Harrow, GB

Download summary PDF View on FDA.gov ↗

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