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FDA 510(k)

Nitronox Scavenger Plus

K-Number: K223452 · 2023-03-05

ApplicantParker Hannifin Corporation
Decision Date2023-03-05
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Nitronox Scavenger Plus is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corporation. It received FDA 510(k) clearance on 2023-03-05 under 510(k) number K223452. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nitronox Scavenger Plus?

Nitronox Scavenger Plus is a medical device that received FDA 510(k) clearance on 2023-03-05. The listed applicant is Parker Hannifin Corporation. The 510(k) number is K223452.

When did Nitronox Scavenger Plus receive FDA 510(k) clearance?

Nitronox Scavenger Plus received FDA 510(k) clearance on 2023-03-05, under 510(k) number K223452.

Who is the listed applicant for Nitronox Scavenger Plus?

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

What is the FDA product code for Nitronox Scavenger Plus?

The FDA product code for Nitronox Scavenger Plus is CBN.

Other records listing Parker Hannifin Corporation 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.

K241465Midas Flowmeter; eAVSK202480Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50K173530Indego(R)K171334IndegoK161731Cleveland Multiport Ventricular Catheter SetK152416Indego

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Related Devices (Code: CBN)

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.

K193646Dynamic Gas Scavenging System 2 (DGSS - 2)Anesthetic Gas Reclamation, Inc.K160950MINISCAVSedation Systems, LLC

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.

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