FDA 510(k)

BD Syringe NRFit Lok and BD Syringe NRFit Slip

N.º K: K192538 · 2020-09-04

SolicitanteBecton, Dickinson and Company

Fecha de decisión2020-09-04

Código de productoQEH

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

BD Syringe NRFit Lok and BD Syringe NRFit Slip is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2020-09-04 under 510(k) number K192538. The device is classified under product code QEH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BD Syringe NRFit Lok and BD Syringe NRFit Slip?

BD Syringe NRFit Lok and BD Syringe NRFit Slip is a medical device that received FDA 510(k) clearance on 2020-09-04. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K192538.

When did BD Syringe NRFit Lok and BD Syringe NRFit Slip receive FDA 510(k) clearance?

BD Syringe NRFit Lok and BD Syringe NRFit Slip received FDA 510(k) clearance on 2020-09-04, under 510(k) number K192538.

Who is the listed applicant for BD Syringe NRFit Lok and BD Syringe NRFit Slip?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Syringe NRFit Lok and BD Syringe NRFit Slip?

The FDA product code for BD Syringe NRFit Lok and BD Syringe NRFit Slip is QEH.

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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.