FDA 510(k)

Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)

N.º K: K244047 · 2025-05-23

Fecha de decisión2025-05-23

Código de productoJKA

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) is the device name listed in this FDA 510(k) record. The listed applicant is Venocare, Inc.. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K244047. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)?

Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Venocare, Inc.. The 510(k) number is K244047.

When did Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) receive FDA 510(k) clearance?

Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) received FDA 510(k) clearance on 2025-05-23, under 510(k) number K244047.

Who is the listed applicant for Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)?

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

What is the FDA product code for Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)?

The FDA product code for Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) is JKA.

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 Venocare, Inc. como solicitante

K260432Ruby Intravascular Catheter K243105Ruby Intravascular Catheter

Dispositivos relacionados (Código: JKA)

K262215Profoject™ Safety Sliding Blood Collection SetCMT Health PTE., Ltd.K252899Female Culture Device; Male Culture Device; Transfer Device; Access DeviceZhejiang Kindly Medical Device Co., Ltd.K260128BD Preset™ and BD A-Line™ Arterial Blood Collection SyringesBecton, Dickinson and Company K252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and Company K252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, Dickinson and Company K252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection TubesBecton, Dickinson and Company

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.