FDA 510(k)

Copa de Prueba de Orina de Drogas Multidroga AllTest; Copa de Prueba de Orina Rápida de Drogas Multidroga AllTest

N.º K: K241428 · 2024-06-17

SolicitanteHangzhou AllTest Biotech Co., Ltd.

Fecha de decisión2024-06-17

Código de productoNFT

Comité asesorTX

DecisiónSubstantially Equivalent

Resumen del dispositivo

AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou AllTest Biotech Co., Ltd.. It received FDA 510(k) clearance on 2024-06-17 under 510(k) number K241428. The device is classified under product code NFT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup?

AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup is a medical device that received FDA 510(k) clearance on 2024-06-17. The listed applicant is Hangzhou AllTest Biotech Co., Ltd.. The 510(k) number is K241428.

When did AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup receive FDA 510(k) clearance?

AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup received FDA 510(k) clearance on 2024-06-17, under 510(k) number K241428.

Who is the listed applicant for AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup?

The FDA 510(k) record lists Hangzhou AllTest Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup?

The FDA product code for AllTest Multi-Drug Urine Test Cup ; AllTest Multi-Drug Rapid Urine Test Cup is NFT.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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

Otros registros que enlistan a Hangzhou AllTest Biotech Co., Ltd. como solicitante

K260342Prueba Rápida de Strep A AllTest K252607Prueba de Infección de Vía Urinaria AllTest K251053Shinetell PlusTM Digital Early Pregnancy Test K250727Copa de Prueba de Orina Rápida de Drogas Multidroga AllTest; Copa de Prueba de Orina de Drogas Multidroga AllTest K242576Medio de Transporte Viral AllTest K244043Copa de Prueba Rápida de Drogas Multidroga AllTest; Copa de Prueba de Drogas Multidroga AllTest

Ver todos los 14 dispositivos →

Dispositivos relacionados (Código: NFT)

K261409BioTeke® Multi-Drug Urine Test CupBioteke Corporation (Wuxi) Co., Ltd.K261984AssureTech Quick Cup Tests;AssureTech Multi-drug Urine Test CupAssure Tech., LLC K261280BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test PanelVivachek Biotech (Hangzhou) Co., Ltd.K260065SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel DxGuangzhou Wondfo Biotech Co., Ltd.K260355Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine CupWEBEST Biotech,, LLC K252550SAFElife T-Cup Multi-Drug Urine Test Cup; SAFElife T-Cup Multi-Drug Urine Test Cup DxGuangzhou Wondfo Biotech Co., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.