510(k) DEN250004 ยท SGX Ultraviolet Light-Based Microbial Reduction Device For Luer-Activated Valves
QIKCAP System
| Applicant | Hai Solutions, Carlsbad CA, US |
| Decision | Unknown, Dec 23, 2025 |
| Received | Jan 30, 2025 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN250004
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.