FDA 510(k)

Bone Marrow Biopsy Needle

Número K: K242322 · 2025-01-24

RequerenteZhejiang Curaway Medical Technology Co., Ltd.

Data da decisão2025-01-24

Código do produtoKNW

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Bone Marrow Biopsy Needle is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Curaway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-01-24 under 510(k) number K242322. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Bone Marrow Biopsy Needle?

Bone Marrow Biopsy Needle is a medical device that received FDA 510(k) clearance on 2025-01-24. The listed applicant is Zhejiang Curaway Medical Technology Co., Ltd.. The 510(k) number is K242322.

When did Bone Marrow Biopsy Needle receive FDA 510(k) clearance?

Bone Marrow Biopsy Needle received FDA 510(k) clearance on 2025-01-24, under 510(k) number K242322.

Who is the listed applicant for Bone Marrow Biopsy Needle?

The FDA 510(k) record lists Zhejiang Curaway Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bone Marrow Biopsy Needle?

The FDA product code for Bone Marrow Biopsy Needle is KNW.

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 Zhejiang Curaway Medical Technology Co., Ltd. como candidato(a)

K260517Automatic Core Biopsy Instrument K244018Disposable Biopsy Needle K241793Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle K240758Radiofrequency Generator System, Cura RF Electrode K232505Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter K222001Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe

Ver todos os 7 dispositivos →

Dispositivos Relacionados (Código: KNW)

K260517Automatic Core Biopsy InstrumentZhejiang Curaway Medical Technology Co., Ltd.K262571EnCor EnCompass™ Breast Biopsy and Tissue Removal SystemBard Peripheral Vascular, Inc.K262792Brevera Biopsy System with CorLumina Imaging Technology (BREVDISP09)Hologic, Inc.K260572Marrow MarxmanMedimetrix, LLC K261196Promisemed VeriEcto Automatic Biopsy NeedlesPromisemed Hangzhou Meditech Co., Ltd.K260365Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Control Module; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Probe, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Disposable Targeting Set, 8 gauge; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Foot Switch; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Reusable Tray; Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Battery CharDevicor Medical Products, Inc.

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.