FDA 510(k)

BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems

N.º K: K161777 · 2016-08-29

SolicitanteBecton Dickinson Infusion Therapy Systems, Inc.

Fecha de decisión2016-08-29

Código de productoFOZ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2016-08-29 under 510(k) number K161777. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems?

BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems is a medical device that received FDA 510(k) clearance on 2016-08-29. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K161777.

When did BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems receive FDA 510(k) clearance?

BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems received FDA 510(k) clearance on 2016-08-29, under 510(k) number K161777.

Who is the listed applicant for BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems?

The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems?

The FDA product code for BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems is FOZ.

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 Becton Dickinson Infusion Therapy Systems, Inc. como solicitante

K252137BD Insyte™ IV Catheter K251422BD Saf-T-Intima™ Subcutaneous Catheter System K243403BD Nexiva™ Closed IV Catheter System K251155BD Cathena™ Safety IV Catheter K251654BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV Catheter K250682BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

Ver todos los 16 dispositivos →

Dispositivos relacionados (Código: FOZ)

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum Vascular K261041ClearSafe Closed SystemMedSource Labs, LLC K260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLC K253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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.