Precision Oxygen Concentrator

FDA 510(k) K072348 · Precision Medical, Inc.

Substantially Equivalent

510(k) numberK072348

Submission

Device name
Precision Oxygen Concentrator
Applicant
Precision Medical, Inc.
Northampton, PA, US
Received
August 21, 2007
Decision date
October 27, 2008
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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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K103324Precision Liquid Oxygen SystemBYJ · Traditional 04/21/2011SE
K090781HELIO2 BlenderBZR · Traditional 08/13/2009SE
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K032018Easy Pulse II Oxygen ConserverNFB · Traditional 08/25/2003SE

Questions and answers

When was Precision Oxygen Concentrator cleared by the FDA?

Precision Oxygen Concentrator (K072348) received a 510(k) decision of Substantially Equivalent on October 27, 2008, 433 days after the submission was received.

What is the product code of K072348?

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