Inogen Rove 4 Portable Oxygen Concentrator

FDA 510(k) K222086 · Inogen

Substantially Equivalent

510(k) numberK222086

Submission

Device name
Inogen Rove 4 Portable Oxygen Concentrator
Applicant
Inogen
Goleta, CA, US
Received
July 15, 2022
Decision date
December 9, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

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Questions and answers

When was Inogen Rove 4 Portable Oxygen Concentrator cleared by the FDA?

Inogen Rove 4 Portable Oxygen Concentrator (K222086) received a 510(k) decision of Substantially Equivalent on December 9, 2022, 147 days after the submission was received.

What is the product code of K222086?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.