Omni 2 Oxygen System

FDA 510(k) K083163 · Sequal Technologies, Inc.

Substantially Equivalent

510(k) numberK083163

Submission

Device name
Omni 2 Oxygen System
Applicant
Sequal Technologies, Inc.
San Diego, CA, US
Received
October 27, 2008
Decision date
October 20, 2009
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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K100920Mesa II Oxygen Concentrator Model: T2000 SeriesCAW · Abbreviated 11/29/2010SE
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Questions and answers

When was Omni 2 Oxygen System cleared by the FDA?

Omni 2 Oxygen System (K083163) received a 510(k) decision of Substantially Equivalent on October 20, 2009, 358 days after the submission was received.

What is the product code of K083163?

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