SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set— 510(k) K222067

Substantially Equivalent

Quanta Dialysis Technologies, Ltd.

FDA 510(k) clearance K222067 for SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set, Substantially Equivalent on 2022-11-10. Applicant: Quanta Dialysis Technologies, Ltd..

Clearance details

Applicant: Quanta Dialysis Technologies, Ltd.
Product code: Code KDI
Advisory panel: Gastroenterology, Urology
Date received: 2022-07-13
Decision date: 2022-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alcester, GB

Download summary PDF View on FDA.gov ↗

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, 2020-01-01 through 2026-04-23. 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.