FDA 510(k)

Nanum Syringe

N.º K: K201930 · 2021-01-17

Fecha de decisión2021-01-17

Código de productoFMF

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Nanum Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Nanum Company Co., Ltd.. It received FDA 510(k) clearance on 2021-01-17 under 510(k) number K201930. 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 Nanum Syringe?

Nanum Syringe is a medical device that received FDA 510(k) clearance on 2021-01-17. The listed applicant is Nanum Company Co., Ltd.. The 510(k) number is K201930.

When did Nanum Syringe receive FDA 510(k) clearance?

Nanum Syringe received FDA 510(k) clearance on 2021-01-17, under 510(k) number K201930.

Who is the listed applicant for Nanum Syringe?

The FDA 510(k) record lists Nanum Company Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nanum Syringe?

The FDA product code for Nanum Syringe is FMF.

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Fuente oficial

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