510(k) K233013 ยท EZL Catheter, Retention Type, Balloon
2-Way 100% Silicone Cleartract Catheter
| Applicant | Silq Technologies Corporation, Sunny Isles Beach FL, US |
| Decision | Substantially Equivalent, Jan 23, 2024 |
| Received | Sep 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233013
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.