FDA 510(k)

Dispositivo de Admixture Direto do Vial para Saco (VDB) sem Agulha Advcare

Número K: K212525 · 2022-08-19

Data da decisão2022-08-19

Código do produtoLHI

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices is the device name listed in this FDA 510(k) record. The listed applicant is Advcare Medical. It received FDA 510(k) clearance on 2022-08-19 under 510(k) number K212525. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices?

Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices is a medical device that received FDA 510(k) clearance on 2022-08-19. The listed applicant is Advcare Medical. The 510(k) number is K212525.

When did Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices receive FDA 510(k) clearance?

Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices received FDA 510(k) clearance on 2022-08-19, under 510(k) number K212525.

Who is the listed applicant for Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices?

The FDA 510(k) record lists Advcare Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices?

The FDA product code for Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices is LHI.

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

Dispositivos Relacionados (Código: LHI)

K252987ADRx® Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LP K251715FlowArt® Vial Access Device VentedAsset Medikal K251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLC K243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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.