HemoCare Hemodialysis System— 510(k) K233557
Substantially EquivalentDeka Research and Development
FDA 510(k) clearance K233557 for HemoCare Hemodialysis System, Substantially Equivalent on 2024-07-12. Applicant: Deka Research and Development.
Clearance details
- Applicant
- Deka Research and Development
- Product code
- Code KDI
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manchester, NH, US
Adverse events under product code KDI
product code KDI- Death
- 352
- Injury
- 1,474
- Malfunction
- 12,534
- Other
- 4
- Total
- 14,364
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.