Genox Model CT-1 Oxygen/Nitrogen Gener-Distr Syst

FDA 510(k) K904002 · Pacific Consolidated Industries

Substantially Equivalent

510(k) numberK904002

Submission

Device name
Genox Model CT-1 Oxygen/Nitrogen Gener-Distr Syst
Applicant
Pacific Consolidated Industries
Orange, CA, US
Received
August 29, 1990
Decision date
September 5, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K100957Deployable Oxygen Concentration System (Docs), Model 66, Deployable Oxygen CeoncentrationCAW · Traditional 01/21/2011SE
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K040738Mobile Oxygen Storage Tank (Most)CAW · Traditional 04/30/2004SE
K020330Deployable Oxygen Concentration System (Docs)CAW · Abbreviated 04/12/2002SE
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Questions and answers

When was Genox Model CT-1 Oxygen/Nitrogen Gener-Distr Syst cleared by the FDA?

Genox Model CT-1 Oxygen/Nitrogen Gener-Distr Syst (K904002) received a 510(k) decision of Substantially Equivalent on September 5, 1990, 7 days after the submission was received.

What is the product code of K904002?

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