FDA 510(k)

Medline Luer Lock Syringes

N.º K: K230235 · 2024-02-16

Fecha de decisión2024-02-16

Código de productoFMF

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Medline Luer Lock Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, LP. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K230235. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Medline Luer Lock Syringes?

Medline Luer Lock Syringes is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Medline Industries, LP. The 510(k) number is K230235.

When did Medline Luer Lock Syringes receive FDA 510(k) clearance?

Medline Luer Lock Syringes received FDA 510(k) clearance on 2024-02-16, under 510(k) number K230235.

Who is the listed applicant for Medline Luer Lock Syringes?

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

What is the FDA product code for Medline Luer Lock Syringes?

The FDA product code for Medline Luer Lock Syringes is FMF.

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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.