Wellead Ureteral Catheter— 510(k) K220036
Substantially EquivalentWell Lead Medical Co., Ltd.
FDA 510(k) clearance K220036 for Wellead Ureteral Catheter, Substantially Equivalent on 2022-12-16. Applicant: Well Lead Medical Co., Ltd..
Clearance details
- Applicant
- Well Lead Medical Co., Ltd.
- Product code
- Code KOD
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Adverse events under product code KOD
product code KOD- Death
- 5
- Injury
- 1,129
- Malfunction
- 7,019
- Total
- 8,153
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.