510(k) K221625 ยท EZL Catheter, Retention Type, Balloon
2-Way 100% Silicone ClearTract Catheter
| Applicant | Silq Technologies Corporation, Sunny Isles Beach FL, US |
| Decision | Substantially Equivalent, Jul 1, 2022 |
| Received | Jun 6, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221625
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.