SGX

Ultraviolet Light-Based Microbial Reduction Device For Luer-Activated Valves

Product code
SGX
Device name
Ultraviolet Light-Based Microbial Reduction Device For Luer-Activated Valves
Device class
Class 2
21 CFR
21 CFR 880.6512
Medical specialty
General Hospital
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
0 (direct download)
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)

FDA classification definition

An ultraviolet light-based microbial reduction device for luer-activated valves is a device that uses ultraviolet light to irradiate luer-activated valves (e.g., as used for intravascular administration). The device is intended to supplement the manual, physical microbicidal treatment of luer-activated valves by providing limited microbial reduction, and is not intended to disinfect or replace manual microbicidal treatment.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2025-12-23.

NumberDecision dateApplicantDevice nameSummary
DEN2500042025-12-23Hai SolutionsQIKCAP System
Official FDA classification page: SGX
Classification and pathway per current FDA publications. Data from openFDA (CC0).