LuMon(TM) System— 510(k) K243765

Substantially Equivalent

Sentec AG

FDA 510(k) clearance K243765 for LuMon(TM) System, Substantially Equivalent on 2025-08-07. Applicant: Sentec AG.

Clearance details

Applicant: Sentec AG
Product code: Code QEB
Advisory panel: Anesthesiology
Date received: 2024-12-06
Decision date: 2025-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Therwil, CH

Download summary PDF View on FDA.gov ↗

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