510(k) K220730 ยท KOD Catheter, Urological
allFlex Ureteral Catheters, Krait Ureteral Catheters
| Applicant | Allwin Medical Devices, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Oct 13, 2022 |
| Received | Mar 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220730
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.