Inovo, Inc. Independence Oxygen Conserving Regulator

FDA 510(k) K051540 · Inovo, Inc.

Substantially Equivalent

510(k) numberK051540

Submission

Device name
Inovo, Inc. Independence Oxygen Conserving Regulator
Applicant
Inovo, Inc.
Naples, FL, US
Received
June 10, 2005
Decision date
September 21, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NFB – Conserver, Oxygen
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5905
Specialty
Anesthesiology

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K113111Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special Inovo, Inc.12/08/2011SE
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More from Chad Therapeutics, Inc.

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K141967Purefill Oxygen CompressorCAW · Traditional 11/07/2014SE
K113111Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special 12/08/2011SE
K103392Chad Therapeutic Evolution Electronic Oxygen ConserverNFB · Special 12/17/2010SE
K060751Inovo, Inc. Accupulse Single Lumen Conserving RegulatorNFB · Traditional 07/18/2006SE
K031983Inovo, Inc, Economizer Conserving RegulatorNFB · Traditional 09/15/2003SE

Questions and answers

When was Inovo, Inc. Independence Oxygen Conserving Regulator cleared by the FDA?

Inovo, Inc. Independence Oxygen Conserving Regulator (K051540) received a 510(k) decision of Substantially Equivalent on September 21, 2005, 103 days after the submission was received.

What is the product code of K051540?

The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.