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FDA 510(k)

Nexiva™ Closed IV Catheter System with NearPort™ IV Access

N.º K: K231239 · 2023-09-22

SolicitanteBecton Dickinson Infusion Therapy Systems, Inc.
Fecha de decisión2023-09-22
Código de productoFOZ
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

Nexiva™ Closed IV Catheter System with NearPort™ IV Access 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 2023-09-22 under 510(k) number K231239. 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 Nexiva™ Closed IV Catheter System with NearPort™ IV Access?

Nexiva™ Closed IV Catheter System with NearPort™ IV Access is a medical device that received FDA 510(k) clearance on 2023-09-22. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K231239.

When did Nexiva™ Closed IV Catheter System with NearPort™ IV Access receive FDA 510(k) clearance?

Nexiva™ Closed IV Catheter System with NearPort™ IV Access received FDA 510(k) clearance on 2023-09-22, under 510(k) number K231239.

Who is the listed applicant for Nexiva™ Closed IV Catheter System with NearPort™ IV Access?

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 Nexiva™ Closed IV Catheter System with NearPort™ IV Access?

The FDA product code for Nexiva™ Closed IV Catheter System with NearPort™ IV Access is FOZ.

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Otros registros que enlistan a Becton Dickinson Infusion Therapy Systems, Inc. como solicitante

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.

K252137BD Insyte™ IV CatheterK251422BD Saf-T-Intima™ Subcutaneous Catheter SystemK243403BD Nexiva™ Closed IV Catheter SystemK251155BD Cathena™ Safety IV CatheterK251654BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV CatheterK250682BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

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Dispositivos relacionados (Código: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan 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.

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