Pogs, Model 65/130

FDA 510(k) K092636 · On Site Gas Systems, Inc.

Substantially Equivalent

510(k) numberK092636

Submission

Device name
Pogs, Model 65/130
Applicant
On Site Gas Systems, Inc.
Newington, CT, US
Received
August 27, 2009
Decision date
January 7, 2010
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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More from Devilbiss Healthcare, LLC

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K063454Pogs, Model 33CCAW · Traditional 05/09/2007SE
K041664Portable Oxygen Generation System: Pogs 33CCAW · Traditional 07/29/2004SE
K030920Pogs 33CAW · Traditional 03/10/2004SE
K021581HemosorbQSY · Traditional 07/12/2002SE
K013390QuickclotQSY · Traditional 05/23/2002SE
K021082On Site Gas Systems Portable Oxygen Generation SYSTEM-1.0 and 5.0CAW · Traditional 05/22/2002SE
K020362P.O.G.S. 3.3 Portable Oxygen Generator SystemCAW · Traditional 02/12/2002SE
K014078On Site Gas Systems Portable Oxygen Generator SystemCAW · Traditional 01/08/2002SE

Questions and answers

When was Pogs, Model 65/130 cleared by the FDA?

Pogs, Model 65/130 (K092636) received a 510(k) decision of Substantially Equivalent on January 7, 2010, 133 days after the submission was received.

What is the product code of K092636?

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