Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
K-Number: K202480 · 2021-04-22
ApplicantParker Hannifin
Decision Date2021-04-22
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is a medical device manufactured by Parker Hannifin. It received FDA 510(k) clearance on 2021-04-22 under approval number K202480. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
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. It is manufactured by Parker Hannifin. The 510(k) number is K202480.
When was Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 approved by the FDA?
Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 received FDA 510(k) clearance on 2021-04-22, under approval number K202480.
What company makes Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50?
Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is manufactured by Parker Hannifin.
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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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.