FDA 510(k)

SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set

Número K: K193670 · 2020-12-23

RequerenteQuanta Dialysis Technologies, Ltd.

Data da decisão2020-12-23

Código do produtoKDI

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set is the device name listed in this FDA 510(k) record. The listed applicant is Quanta Dialysis Technologies, Ltd.. It received FDA 510(k) clearance on 2020-12-23 under 510(k) number K193670. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set is a medical device that received FDA 510(k) clearance on 2020-12-23. The listed applicant is Quanta Dialysis Technologies, Ltd.. The 510(k) number is K193670.

When did SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set receive FDA 510(k) clearance?

SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set received FDA 510(k) clearance on 2020-12-23, under 510(k) number K193670.

Who is the listed applicant for SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

The FDA 510(k) record lists Quanta Dialysis Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

The FDA product code for SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set is KDI.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Outros registros que listam Quanta Dialysis Technologies, Ltd. como candidato(a)

K242269SC+ Hemodialysis Device (SC-14269); Dialysate Cartridge (SC-14656); Blood Tube Set (SC-14651)K222067SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set K210661SC+ Hemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tubeset

Dispositivos Relacionados (Código: KDI)

K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLC K252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLC K260533ELISIO™-HNipro Medical Corporation K252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLC K253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLC

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.