FDA 510(k)

BD Cathena Safety IV Catheter

N.º K: K220584 · 2022-03-31

SolicitanteBecton Dickinson Infusion Therapy Systems, Inc.

Fecha de decisión2022-03-31

Código de productoFOZ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

BD Cathena Safety IV Catheter 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 2022-03-31 under 510(k) number K220584. 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 Cathena Safety IV Catheter?

BD Cathena Safety IV Catheter is a medical device that received FDA 510(k) clearance on 2022-03-31. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K220584.

When did BD Cathena Safety IV Catheter receive FDA 510(k) clearance?

BD Cathena Safety IV Catheter received FDA 510(k) clearance on 2022-03-31, under 510(k) number K220584.

Who is the listed applicant for BD Cathena Safety IV Catheter?

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 Cathena Safety IV Catheter?

The FDA product code for BD Cathena Safety IV Catheter is FOZ.

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

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Dispositivos relacionados (Código: FOZ)

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Fuente oficial

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