510(k) K241734 · GBM Catheter, Urethral
Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter Compact
| Applicant | Well Lead Medical Co., Ltd., Guangzhou, CN |
| Decision | Substantially Equivalent, Mar 5, 2025 |
| Received | Jun 17, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241734
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.