FDA 510(k)

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle

N.º K: K222852 · 2023-05-25

Fecha de decisión2023-05-25

Código de productoFMI

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corporation. It received FDA 510(k) clearance on 2023-05-25 under 510(k) number K222852. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is a medical device that received FDA 510(k) clearance on 2023-05-25. The listed applicant is Nipro Medical Corporation. The 510(k) number is K222852.

When did Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle receive FDA 510(k) clearance?

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle received FDA 510(k) clearance on 2023-05-25, under 510(k) number K222852.

Who is the listed applicant for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

The FDA 510(k) record lists Nipro Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

The FDA product code for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is FMI.

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Dispositivos relacionados (Código: FMI)

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Fuente oficial

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