FDA 510(k)

Insulin syringe with integrated needle DL

Número K: K203211 · 2023-02-09

Data da decisão2023-02-09

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Insulin syringe with integrated needle DL is the device name listed in this FDA 510(k) record. The listed applicant is Dlp Medical Products, Corp.. It received FDA 510(k) clearance on 2023-02-09 under 510(k) number K203211. 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 Insulin syringe with integrated needle DL?

Insulin syringe with integrated needle DL is a medical device that received FDA 510(k) clearance on 2023-02-09. The listed applicant is Dlp Medical Products, Corp.. The 510(k) number is K203211.

When did Insulin syringe with integrated needle DL receive FDA 510(k) clearance?

Insulin syringe with integrated needle DL received FDA 510(k) clearance on 2023-02-09, under 510(k) number K203211.

Who is the listed applicant for Insulin syringe with integrated needle DL?

The FDA 510(k) record lists Dlp Medical Products, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Insulin syringe with integrated needle DL?

The FDA product code for Insulin syringe with integrated needle DL is FMF.

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Fonte oficial

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