SGX
- 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.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN250004 | 2025-12-23 | Hai Solutions | QIKCAP System | — |
Official FDA classification page: SGX
Classification and pathway per current FDA publications. Data from openFDA (CC0).