FDA 510(k)

Medline Luer Lock Syringes

Número K: K230235 · 2024-02-16

Data da decisão2024-02-16

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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Fonte oficial

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