FDA 510(k)

SafeR Syringe and SafeR Sting

N.º K: K221981 · 2022-12-29

Fecha de decisión2022-12-29

Código de productoMEG

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

SafeR Syringe and SafeR Sting is the device name listed in this FDA 510(k) record. The listed applicant is Roncadelle Operations Srl. It received FDA 510(k) clearance on 2022-12-29 under 510(k) number K221981. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SafeR Syringe and SafeR Sting?

SafeR Syringe and SafeR Sting is a medical device that received FDA 510(k) clearance on 2022-12-29. The listed applicant is Roncadelle Operations Srl. The 510(k) number is K221981.

When did SafeR Syringe and SafeR Sting receive FDA 510(k) clearance?

SafeR Syringe and SafeR Sting received FDA 510(k) clearance on 2022-12-29, under 510(k) number K221981.

Who is the listed applicant for SafeR Syringe and SafeR Sting?

The FDA 510(k) record lists Roncadelle Operations Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SafeR Syringe and SafeR Sting?

The FDA product code for SafeR Syringe and SafeR Sting is MEG.

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Fuente oficial

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