Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
K-Number: K202480 · 2021-04-22
Device Summary
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. 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.
Other records listing Parker Hannifin as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BZR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.