FDA 510(k)

Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50

Número K: K202480 · 2021-04-22

Data da decisão2021-04-22

Código do produtoBZR

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin. It received FDA 510(k) clearance on 2021-04-22 under 510(k) number K202480. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50?

Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is a medical device that received FDA 510(k) clearance on 2021-04-22. The listed applicant is Parker Hannifin. The 510(k) number is K202480.

When did Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 receive FDA 510(k) clearance?

Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 received FDA 510(k) clearance on 2021-04-22, under 510(k) number K202480.

Who is the listed applicant for Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50?

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

What is the FDA product code for Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50?

The FDA product code for Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is BZR.

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